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Testosterone Effects on Short-Term Physical, Hormonal, and Neurodevelopmental Outcomes (TESTO) in Infants with 47,XXY; The Journal of Clinical Endocrinology & Metabolism; (2025).

An extra X chromosome among adult women in the Million Veteran Program: A more benign perspective of trisomy X; American Journal of Medical Genetics Part C: Seminars in Medical Genetics; (2024).

Research Priorities of Individuals and Families with Sex Chromosome Aneuploidies; Unknown Source; (2024).

Testosterone Effects on Short-Term Physical, Hormonal, and Neurodevelopmental Outcomes in Infants with 47,XXY/Klinefelter Syndrome: The TESTO Randomized Controlled Trial; Unknown Source; (2024).

Capacity Building in a New Clinical Trials Network through Inter-Network Collaboration; Journal of Pediatrics; (2022).

Non-invasive prenatal testing (NIPT) results for participants of the extraordinary babies study: Screening, counseling, diagnosis, and discordance; medRxiv; (2021).

Long-Term Safety of Growth Hormone Treatment in Childhood: Two Large Observational Studies: NordiNet IOS and ANSWER; Journal of Clinical Endocrinology and Metabolism; (2021).

Long-Term Effectiveness and Safety of Childhood Growth Hormone Treatment in Noonan Syndrome; Hormone Research in Paediatrics; (2021).

Erratum: Variation in early number skills and mathematics achievement: Implications from cognitive profiles of children with or without Turner syndrome (PLoS ONE (2020) 15:10 (e0239224) DOI: 10.1371/journal.pone.0239224); PLoS ONE; (2021).

Decreased levels of γ-aminobutyric acid in temporal lobe of children with 47,XYY syndrome; NeuroReport; (2021).

Congenital Causes of Hypergonadotropic Hypogonadism: Anorchia and Klinefelter Syndrome; Trends in Andrology and Sexual Medicine; (2021).

Phenobarbital and clonidine as secondary medications for neonatal opioid withdrawal syndrome; Pediatrics; (2021).

Prevention of Growth Failure in Turner Syndrome: Long-Term Results of Early Growth Hormone Treatment in the "toddler Turner" Cohort; Hormone Research in Paediatrics; (2021).

Consensus Parameter: Research Methodologies to Evaluate Neurodevelopmental Effects of Pubertal Suppression in Transgender Youth; Transgender Health; (2020).

Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention; American Journal of Medical Genetics, Part C: Seminars in Medical Genetics; (2020).

IDeA States Pediatric Clinical Trials Network for Underserved and Rural Communities; Pediatrics; (2020).

Minipuberty in Klinefelter syndrome: Current status and future directions; American Journal of Medical Genetics, Part C: Seminars in Medical Genetics; (2020).

Once-Weekly somapacitan vs daily GH in children with GH deficiency: Results from a randomized phase 2 trial; Journal of Clinical Endocrinology and Metabolism; (2020).

Sensory Features as a Marker of Autism Spectrum Disorders; Journal of Autism and Developmental Disorders; (2020).

Testicular function in boys with 47,XYY and relationship to phenotype; American Journal of Medical Genetics, Part C: Seminars in Medical Genetics; (2020).

Ultra-low-dose estrogen therapy for female hypogonadism; Clinical Pediatric Endocrinology; (2020).

Variation in early number skills and mathematics achievement: Implications from cognitive profiles of children with or without Turner syndrome; PLoS ONE; (2020).

Abnormal Auditory Mismatch Fields in Children and Adolescents with 47,XYY Syndrome; Developmental Neuroscience; (2019).

Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression; American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics; (2019).

Abnormal maturation of the resting-state peak alpha frequency in children with autism spectrum disorder; Human Brain Mapping; (2019).

Treatment of Children with GH in the United States and Europe: Long-Term Follow-Up from NordiNet^® IOS and ANSWER Program; Journal of Clinical Endocrinology and Metabolism; (2019).

Quality of Life in Adolescent Boys with Idiopathic Short Stature: Positive Impact of Growth Hormone and Aromatase Inhibitors; Hormone Research in Paediatrics; (2019).

Psychometric performance of the Quality of Life in Short Stature Youth (QoLISSY) questionnaire in a randomized open-label comparator trial in idiopathic short stature; Journal of Pediatric Endocrinology and Metabolism; (2019).

Prenatal opioid exposure: Neurodevelopmental consequences and future research priorities; Pediatrics; (2019).

Impact of route of administration on genotoxic oestrogens concentrations using oral vs transdermal oestradiol in girls with Turner syndrome; Clinical Endocrinology; (2019).

Height Gain and Safety Outcomes in Growth Hormone-Treated Children with Idiopathic Short Stature: Experience from a Prospective Observational Study; Hormone Research in Paediatrics; (2019).

Brain Development in School-Age and Adolescent Girls: Effects of Turner Syndrome, Estrogen Therapy, and Genomic Imprinting; Biological Psychiatry; (2019).

Auditory evoked response delays in children with 47,XYY syndrome; NeuroReport; (2019).

Androgen treatment effects on hippocampus structure in boys with Klinefelter syndrome; Psychoneuroendocrinology; (2019).

Oxandrolone Treatment Results in an Increased Risk of Gonadarche in Prepubertal Boys with Klinefelter Syndrome; Journal of Clinical Endocrinology and Metabolism; (2018).

Three years of growth hormone therapy in children born small for gestational age: Results from the answer program; Endocrine Connections; (2018).

Sex-chromosome dosage effects on gene expression in humans; Proceedings of the National Academy of Sciences of the United States of America; (2018).

Klinefelter syndrome; Encyclopedia of Endocrine Diseases; (2018).

Growth Hormone Treatment for Short Stature in the USA, Germany and France: 15 Years of Surveillance in the Genetics and Neuroendocrinology of Short-Stature International Study (GeNeSIS); Hormone Research in Paediatrics; (2018).

Electronically Verified Use of Internet-Based, Multimedia Decision Aids by Adolescents With Type 1 Diabetes and Their Caregivers; MDM Policy and Practice; (2018).

Safety Outcomes and Near-Adult Height Gain of Growth Hormone-Treated Children with SHOX Deficiency: Data from an Observational Study and a Clinical Trial; Hormone Research in Paediatrics; (2017).

Identification of 15 novel partial SHOX deletions and 13 partial duplications, and a review of the literature reveals intron 3 to be a hotspot region; Journal of Human Genetics; (2017).

Effects of oxandrolone on cardiometabolic health in boys with klinefelter syndrome: A randomized controlled trial; Journal of Clinical Endocrinology and Metabolism; (2017).

Clinical practice guidelines for the care of girls and women with Turner syndrome: Proceedings from the 2016 Cincinnati International Turner Syndrome Meeting; European Journal of Endocrinology; (2017).

Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYY; Journal of Developmental and Behavioral Pediatrics; (2017).

Androgen Treatment Effects on Motor Function, Cognition, and Behavior in Boys with Klinefelter Syndrome; Journal of Pediatrics; (2017).

The ups and downs of parenting young children with type 1 diabetes: A crowdsourcing study; Journal of Pediatric Psychology; (2017).

Sex chromosome dosage effects on gene expression in humans; bioRxiv; (2017).

Consideration of Insulin Pumps or Continuous Glucose Monitors by Adolescents With Type 1 Diabetes and Their Parents: Stakeholder Engagement in the Design of Web-Based Decision Aids; Diabetes Educator; (2016).

Advances in the Interdisciplinary Care of Children with Klinefelter Syndrome; Advances in Pediatrics; (2016).

Randomized trial of aromatase inhibitors, growth hormone, or combination in pubertal boys with idiopathic, short stature; Journal of Clinical Endocrinology and Metabolism; (2016).

Growth Hormone Research Society perspective on the development of long-acting growth hormone preparations; European Journal of Endocrinology; (2016).

Gonadal function is associated with cardiometabolic health in pre-pubertal boys with Klinefelter syndrome; Andrology; (2016).

A randomized, double blind, placebo-controlled pilot trial of the safety and efficacy of atorvastatin in children with elevated low-density lipoprotein cholesterol (LDL-C) and type 1 diabetes; Pediatric Diabetes; (2015).

Radiological features in patients with short stature homeobox-containing (SHOX) gene deficiency and turner syndrome before and after 2 years of gh treatment; Hormone Research in Paediatrics; (2015).

Magnetic resonance imaging measures of decreased aortic strain and distensibility are proportionate to insulin resistance in adolescents with type 1 diabetes mellitus; Pediatric Diabetes; (2015).

Evaluation of the american-english quality of life in short stature youth (QoLISSY) questionnaire in the United States; Health and Quality of Life Outcomes; (2015).

Commentary: Launch of a quality improvement network for evidence-based management of uncommon pediatric endocrine disorders: Turner syndrome as a prototype; Journal of Clinical Endocrinology and Metabolism; (2015).

Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features; Genes, Brain and Behavior; (2015).

Attaining genetic height potential: Analysis of height outcomes from the ANSWER Program in children treated with growth hormone over 5 years; Growth Hormone and IGF Research; (2015).

Testis Development and Fertility Potential in Boys with Klinefelter Syndrome; Endocrinology and Metabolism Clinics of North America; (2015).

A multicenter, open-label, observational study of testosterone gel (1%) in the treatment of adolescent boys with klinefelter syndrome or anorchia; Journal of Adolescent Health; (2014).

Influence of the X-chromosome on neuroanatomy: Evidence from turner and klinefelter syndromes; Journal of Neuroscience; (2014).

Safety and efficacy of oxandrolone in growth hormone-treated girls with turner syndrome: Evidence from recent studies and recommendations for use; Hormone Research in Paediatrics; (2014).

Effects of low-dose estrogen replacement during childhood on pubertal development and gonadotropin concentrations in patients with turner syndrome: Results of a randomized, double-blind, placebo-controlled clinical trial; Journal of Clinical Endocrinology and Metabolism; (2014).

Brain morphology in children with 47,XYY syndrome: A voxel- and surface-based morphometric study; Genes, Brain and Behavior; (2014).

Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes; Journal of Neurodevelopmental Disorders; (2014).

Contextualized analysis of a needs assessment using the Theoretical Domains Framework: A case example in endocrinology; BMC Health Services Research; (2014).

47,XYY syndrome: Clinical phenotype and timing of ascertainment; Journal of Pediatrics; (2013).

Erratum: GH Treatment to final height produces similar height gains in patients with shox deficiency and turner syndrome: Results of a multicenter trial (Journal of Clinical Endocrinology and Metabolism (2013) 98 (E1383-E1392) DOI:10.1210/jc.2013-1222); Journal of Clinical Endocrinology and Metabolism; (2013).

GH treatment to final height produces similar height gains in patients with SHOX deficiency and turner syndrome: Results of a multicenter trial; Journal of Clinical Endocrinology and Metabolism; (2013).

The NordiNet® International Outcome Study and NovoNet® ANSWER Program®: Rationale, design, and methodology of two international pharmacoepidemiological registry-based studies monitoring long-term clinical and safety outcomes of growth hormone therapy (Norditropin®); Clinical Epidemiology; (2013).

Metabolic effects of oral versus transdermal 17β-estradiol (E ₂): A randomized clinical trial in girls with turner syndrome; Journal of Clinical Endocrinology and Metabolism; (2013).

Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY klinefelter syndrome; Pediatrics; (2012).

C-type natriuretic peptide (CNP) levels are altered in boys with Klinefelter syndrome; Journal of Clinical Endocrinology and Metabolism; (2012).

Social deficits in male children and adolescents with sex chromosome aneuploidy: A comparison of XXY, XYY, and XXYY syndromes; Research in Developmental Disabilities; (2012).

Sex chromosomes and the brain: A study of neuroanatomy in XYY syndrome; Developmental Medicine and Child Neurology; (2012).

Gender influences short-term growth hormone treatment response in children; Hormone Research in Paediatrics; (2012).

Clinical and hormonal status of infants with nonmosaic XXY karyotype; Acta Paediatrica, International Journal of Paediatrics; (2011).

Prospective study confirms oxandrolone-associated improvement in height in growth hormone-treated adolescent girls with turner syndrome; Hormone Research in Paediatrics; (2011).

Neuroanatomical phenotype of klinefelter syndrome in childhood: A voxel-based morphometry study; Journal of Neuroscience; (2011).

Insulin resistance and metabolic syndrome in prepubertal boys with Klinefelter syndrome; Acta Paediatrica, International Journal of Paediatrics; (2011).

Impact of age and duration of growth hormone therapy in Children with turner syndrome; Hormone Research in Paediatrics; (2011).

Growth hormone plus childhood low-dose estrogen in turner syndrome; Obstetrical and Gynecological Survey; (2011).

Growth hormone plus childhood low-dose estrogen in Turner's syndrome; New England Journal of Medicine; (2011).

Clinical and molecular evaluation of SHOX/PAR1 duplications in léri-weill dyschondrosteosis (LWD) and idiopathic short stature (ISS); Journal of Clinical Endocrinology and Metabolism; (2011).

Assessment of leydig and sertoli cell functions in infants with nonmosaic klinefelter syndrome: Insulin-like peptide 3 levels are normal and positively correlated with lh levels; Journal of Clinical Endocrinology and Metabolism; (2011).

Atypical functional brain activation during a multiple object tracking task in girls with turner syndrome: Neurocorrelates of reduced spatiotemporal resolution; American Journal on Intellectual and Developmental Disabilities; (2010).

Cortical anatomy in human X monosomy; NeuroImage; (2010).

Erratum to Cortical anatomy in human X monosomy [NeuroImage, 49, (2010), 2915-2923]; NeuroImage; (2010).

Growth hormone: Health considerations beyond height gain; Pediatrics; (2010).

An extra X or Y chromosome: Contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome; Developmental Disabilities Research Reviews; (2009).

Effects of Treatment with Oxandrolone for 4 Years on the Frequency of Severe Arithmetic Learning Disability in Girls with Turner Syndrome; Journal of Pediatrics; (2009).

Height gains in response to growth hormone treatment to final height are similar in patients with SHOX deficiency and Turner syndrome; Hormone Research; (2009).

Introduction: Cognitive profiles in sex chromosome disorders; Developmental Disabilities Research Reviews; (2009).

Structural and functional neuroimaging in Klinefelter (47,XXY) syndrome: A review of the literature and preliminary results from a functional magnetic resonance imaging study of language; Developmental Disabilities Research Reviews; (2009).

Cognitive and motor development during childhood in boys with Klinefelter syndrome; American Journal of Medical Genetics, Part A; (2008).

A new look at XXYY syndrome: Medical and psychological features; American Journal of Medical Genetics, Part A; (2008).

Consensus statement on the diagnosis and treatment of children with idiopathic short stature: A summary of the Growth Hormone Research Society, the Lawson Wilkins Pediatric Endocrine Society, and the European Society for Paediatric Endocrinology Workshop; Journal of Clinical Endocrinology and Metabolism; (2008).

EFHC2 SNP rs7055196 is not associated with fear recognition in 45,X Turner syndrome; American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics; (2008).

Effect of Ascertainment and Genetic Features on the Phenotype of Klinefelter Syndrome; Journal of Pediatrics; (2008).

Overlapping numerical cognition impairments in children with chromosome 22q11.2 deletion or Turner syndromes; Neuropsychologia; (2008).

Idiopathic short stature: Management and growth hormone treatment; Growth Hormone and IGF Research; (2008).

Growth hormone treatment of early growth failure in toddlers with turner syndrome: A randomized, controlled, multicenter trial; Journal of Clinical Endocrinology and Metabolism; (2007).

Growth hormone is effective in treatment of short stature associated with short stature homeobox-containing gene deficiency: Two-year results of a randomized, controlled, multicenter trial; Journal of Clinical Endocrinology and Metabolism; (2007).

Genotypes and phenotypes in children with short stature: Clinical indicators of SHOX haploinsufficiency; Journal of Medical Genetics; (2007).

Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD); American Journal of Medical Genetics, Part A; (2007).

A turner syndrome neurocognitive phenotype maps to Xp22.3; Behavioral and Brain Functions; (2007).

Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effects; Journal of Pediatric Psychology; (2006).

Differences in follicle-stimulating hormone secretion between 45,X monosomy Turner syndrome and 45,X/46,XX mosaicism are evident at an early age; Journal of Clinical Endocrinology and Metabolism; (2006).

Cognition and the sex chromosomes: Studies in Turner syndrome; Hormone Research; (2006).

A second recombination hotspot associated with SHOX deletions [2]; American Journal of Human Genetics; (2006).

Language use in females with fragile X or turner syndrome during brief initial social interactions; Journal of Developmental and Behavioral Pediatrics; (2006).

Reply to Benito-Sanz et al.; American Journal of Human Genetics; (2006).

Shyness, social anxiety, and impaired self-esteem in Turner syndrome and premature ovarian failure [2]; Journal of the American Medical Association; (2006).

Effects of growth hormone on cognitive function; Hormone Research; (2005).

Androgen receptor CAG_n repeat length influences phenotype of 47,XXY (Klinefelter) syndrome; Journal of Clinical Endocrinology and Metabolism; (2005).

Early androgen deficiency in infants and young boys with 47,XXY Klinefelter syndrome; Hormone Research; (2005).

Safety of growth hormone treatment in pediatric patients with idiopathic short stature; Journal of Clinical Endocrinology and Metabolism; (2005).

The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: Contrasting children with Leri-Weill dyschondrosteosis and turner syndrome; Journal of Pediatrics; (2005).

Effect of growth hormone treatment on adult height in peripubertal children with idiopathic short stature: A randomized, double-blind, placebo-controlled trial; Journal of Clinical Endocrinology and Metabolism; (2004).

Hypodense nodularity on computed tomography: Novel imaging and pathology of micronodular adrenocortical hyperplasia associated with myelolipomatous changes; Journal of Clinical Endocrinology and Metabolism; (2004).

The effect of genetic differences and ovarian failure: Intact cognitive function in adult women with premature ovarian failure versus turner syndrome; Journal of Clinical Endocrinology and Metabolism; (2004).

Psychological adaptation in children with idiopathic short stature treated with growth hormone or placebo; Journal of Clinical Endocrinology and Metabolism; (2004).

Phenotype and X inactivation in 45,X/46,X,r(X) cases; American Journal of Medical Genetics; (2004).

Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasia; American Journal of Medical Genetics; (2003).

Estradiol levels in girls with Turner's syndrome compared to normal prepubertal girls as determined by an ultrasensitive assay; Journal of Pediatric Endocrinology and Metabolism; (2003).

Androgen-responsive aspects of cognition in girls with turner syndrome; Journal of Clinical Endocrinology and Metabolism; (2003).

Behavioral assessment of social anxiety in females with turner or fragile X syndrome; Journal of Autism and Developmental Disorders; (2003).

A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD; American Journal of Medical Genetics; (2003).

Author‘ Response: SHOX-A Geneticist‘s View; Journal of Clinical Endocrinology and Metabolism; (2002).

Brain development in Turner syndrome: A magnetic resonance imaging study; Psychiatry Research - Neuroimaging; (2002).

Complete SHOX deficiency causes Langer mesomelic dysplasia; American Journal of Medical Genetics; (2002).

Dysmetabolic syndrome: multiple risk factors for premature adult disease in an adolescent girl.; Pediatrics; (2002).

Persistent cognitive deficits in adult women with Turner syndrome; Neurology; (2002).

A man who inherited his SRY gene and Leri-Weill dyschondrosteosis from his mother and neurofibromatosis type 1 from his father; American Journal of Medical Genetics; (2001).

Phenotypes associated with SHOX deficiency; Journal of Clinical Endocrinology and Metabolism; (2001).

Psychosocial development in adolescents with Turner syndrome; Journal of Developmental and Behavioral Pediatrics; (2001).

Molecular analysis of genes on Xp controlling Turner syndrome and premature ovarian failure (POF); Seminars in Reproductive Medicine; (2001).

Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene; Cytogenetics and Cell Genetics; (2000).

Neurodevelopmental and psychosocial aspects of turner syndrome; Mental Retardation and Developmental Disabilities Research Reviews; (2000).

The turner syndrome-associated neurocognitive phenotype maps to distal Xp; American Journal of Human Genetics; (2000).

Use of estrogen in young girls with Turner syndrome: Effects on memory; Neurology; (2000).

Turner syndrome and haploinsufficiency; Current Opinion in Genetics and Development; (1998).

Effects of estrogen on nonverbal processing speed and motor function in girls with Turner's syndrome; Journal of Clinical Endocrinology and Metabolism; (1998).

Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1; American Journal of Human Genetics; (1998).

Transition to young adulthood in Ullrich-Turner syndrome: Neurodevelopmental changes; American Journal of Medical Genetics; (1998).

Del(X)(p21.2) in a mother and two daughters with variable ovarian function; Clinical Genetics; (1997).

Discriminant analysis of the Ullrich-Turner syndrome neurocognitive profile; American Journal of Medical Genetics; (1997).

Absence of Growth Hormone Effects on Cognitive Function in Girls with Turner Syndrome; Journal of Clinical Endocrinology and Metabolism; (1997).

Syndromes and arthritis; Rheumatic Disease Clinics of North America; (1997).

Search for the Turner gene; Clinical Pediatric Endocrinology; (1997).

Neuroblastoma and related tumors in Turner's syndrome; Journal of Pediatrics; (1997).

Executive Function in Girls with Turner's Syndrome; Developmental Neuropsychology; (1997).

Self-concept and behavior in adolescent girls with Turner syndrome: Potential estrogen effects; Journal of Clinical Endocrinology and Metabolism; (1996).

Erratum: Self-concept and behavior in adolescent girls with Turner syndrome: Potential estrogen effects (Journal of Clinical Endocrinology and Metabolism (1996) 81 (926-931)); Journal of Clinical Endocrinology and Metabolism; (1996).

Developmental changes in motor function in girls with Turner syndrome; Pediatric Neurology; (1996).

Brain development, gender and IQ in children. A volumetric imaging study; Brain; (1996).

Neurodevelopmental effects of X monosomy: A volumetric imaging study; Annals of Neurology; (1995).

Lipid abnormalities in Turner syndrome; The Journal of Pediatrics; (1995).

Growth hormone hypersecretion in a girl with McCune-Albright syndrome: Comparison with controls and response to a dose of long-acting somatostatin analog; Journal of Clinical Endocrinology and Metabolism; (1995).

Self-Esteem and Behavior in Girls with Turner Syndrome; Journal of Developmental and Behavioral Pediatrics; (1995).

Ullrich-Turner syndrome: Neurodevelopmental changes from childhood through adolescence; American Journal of Medical Genetics; (1995).

Pubertal Changes in Bone Mineral Content of The Wrist and Spine in Normal Boys and Girls; Clinical Pediatric Endocrinology; (1994).

Altered brain development in turner's syndrome: An event-related potential study; Neurology; (1993).

Neurocognitive function and brain imaging in turner syndrome - preliminary results; Hormone Research in Paediatrics; (1993).

Estrogen Therapy in Turner's Syndrome; Pediatrics International; (1992).

Spontaneous growth hormone secretion increases during puberty in normal girls and boys; Pediatric Nephrology; (1992).

The optimal use of estrogen in the treatment of turner's syndrome; Endocrinologist; (1992).

Spontaneous Growth Hormone Secretion Increases during Puberty in Normal Girls and Boys; Journal of Clinical Endocrinology and Metabolism; (1991).

Normal bone density of the wrist and spine and increased wrist fractures in girls with turner's syndrome; Journal of Clinical Endocrinology and Metabolism; (1991).

Solitary polyclonal autonomous thyroid nodule: A rare cause of childhood hyperthyroidism; Journal of Clinical Endocrinology and Metabolism; (1991).

Measurement of short‐term growth with a new knee height measuring device; American Journal of Human Biology; (1989).

The effect of short term treatment with growth hormone and ethinyl estradiol on lower leg growth rate in girls with turner's syndrome; Journal of Clinical Endocrinology and Metabolism; (1988).

The Advantage of Measuring Stimulated as Compared with Spontaneous Growth Hormone Levels in the Diagnosis of Growth Hormone Deficiency; New England Journal of Medicine; (1988).

Stimulated as Compared with Spontaneous Growth Hormone Levels for Diagnosis of Growth Hormone Deficiency; New England Journal of Medicine; (1988).

Abnormal growth hormone secretory dynamics in children with familial hypercholesterolemia; Hormone Research; (1988).

Growth hormone secretory dynamics in children with precocious puberty; The Journal of Pediatrics; (1987).

Ultrasonography of Turner's syndrome; Journal of Ultrasound in Medicine; (1986).

Pubertal growth: physiology and pathophysiology.; Recent progress in hormone research; (1986).

Ovine Corticotropin-Releasing Hormone Stimulation Test in Normal Children; Journal of Clinical Endocrinology and Metabolism; (1986).

Growth response relationship between growth hormone dose and short term growth in patients with turner's syndrome; Journal of Clinical Endocrinology and Metabolism; (1986).

Growth Hormone (GH) responses to gh-releasing hormone during pubertal development in normal boys and girls: Comparison to idiopathic short stature and GH deficiency; Journal of Clinical Endocrinology and Metabolism; (1986).

Effect of low doses of estradiol on 6-month growth rates and predicted height in patients with Turner syndrome; The Journal of Pediatrics; (1986).

Reply; The Journal of Pediatrics; (1985).

Growth hormone secretory dynamics in Turner syndrome; The Journal of Pediatrics; (1985).

Effects of pulsatile administration of growth hormone (GH)-releasing hormone on short term linear growth in children with GH deficiency; Journal of Clinical Endocrinology and Metabolism; (1985).

Short term, low dose estradiol accelerates ulnar growth in boys; Journal of Clinical Endocrinology and Metabolism; (1985).

A comparison of two methods for detecting hormone peaks: The effect of sampling interval on gonadotropin peak frequency; Journal of Clinical Endocrinology and Metabolism; (1984).

A preliminary study of the effect of estrogen dose on growth in turner's syndrome; Obstetrical and Gynecological Survey; (1984).

Absence of pubertal gonadotropin secretion in girls with mccune-albright syndrome; Journal of Clinical Endocrinology and Metabolism; (1984).

Developmental changes in neuroendocrine regulation of gonadotropin secretion in gonadal dysgenesis; Obstetrical and Gynecological Survey; (1984).

Ocular Findings in Turner Syndrome: A Prospective Study; Ophthalmology; (1984).

Variable response to a long-acting agonist of luteinizing hormone-releasing hormone in girls with mccune-albright syndrome; Journal of Clinical Endocrinology and Metabolism; (1984).

A Preliminary Study of the Effect of Estrogen Dose on Growth in Turner's Syndrome; New England Journal of Medicine; (1983).

Developmental changes in neuroendocrine regulation of gonadotropin secretion in gonadal dysgenesis; Journal of Clinical Endocrinology and Metabolism; (1983).