SelmaFWitchelMD

Associate Professor, Pediatrics, University of Pittsburgh School of Medicine

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Office
3414 5th Ave
Bldg
Pittsburgh, PA 15213
Phone+1 412-692-5170

Fax+1 412-692-5834

UPMC Medical EducationFellowship, Endocrinology, Diabetes, and Metabolism, 1981 - 1983
Cincinnati Children's Hospital Medical CenterResidency, Pediatrics, 1979 - 1981
Cincinnati Children's Hospital Medical CenterInternship, Pediatrics, 1978 - 1979
University of Pittsburgh School of MedicineClass of 1978

PubMed

Recurrent Xp22.31-Yq11 Unbalanced Translocations: Molecular Diagnosis and Clinical Implications in Three Families.
Marwa Daghsni, Elizabeth Sheehan, Suneeta Madan-Khetarpal, Mahmoud Aarabi, Selma F Witchel
American Journal of Medical Genetics. Part A. 2024-10-23
1 citations
Prevalence and accurate diagnosis of polycystic ovary syndrome in adolescents across world regions: a systematic review and meta-analysis.
Adriana C H Neven, Maria Forslund, Sanjeeva Ranashinha, Aya Mousa, Chau Thien Tay
European Journal of Endocrinology. 2024-09-30
Response to Letter to the Editor From de Zegher and Ibáñez: "Metformin and Combined Oral Contraceptive Pills in the Management of Polycystic Ovary Syndrome: A Systemat...
Johanna Melin, Maria Forslund, Simon Alesi, Terhi Piltonen, Daniela Romualdi
The Journal of Clinical Endocrinology and Metabolism. 2024-09-16

Lectures

Neuroendocrine Control of the Onset of PubertyApril 22nd, 2020
For Future Offspring, Docs Save Eggs from Teen Transitioning Female-to-MaleFebruary 27th, 2019

Studies Of Abnormal Sexual Differentiation And Development:Serum Inhibin B &FshNational Center For Research Resources2004–2005
Molecular Diagnosis Of Congenital Adrenal Hyperplasia: Phenotype/GenotypeNational Center For Research Resources2004–2005
Evaluation &Treatment Of Abnormalities Of Gonadal Or Pubertal DevelopmentNational Center For Research Resources2004–2005
Steroidogenesis In HyperandrogenismNational Center For Research Resources1996–2005
Molecular Diagnosis Of Congenital Adrenal Hyperplasia--Phenotype/GenotpeNational Center For Research Resources1998–2002
Chronic Anovulatory Hyperandrogenism: Sorting GenotypesEunice Kennedy Shriver National Institute Of Child Health &Human Development1997–2001
21 Hydroxylase Deficiency Congenital Adrenal HyperplasiaNational Center For Research Resources1996–1997
Growth Hormone Therapy In Kidney DiseaseNational Center For Research Resources1996
Gene Mutation In 21-Hydroxylase DeficiencyEunice Kennedy Shriver National Institute Of Child Health &Human Development1992–1996