Sekizkardes, Hilal
17  results:
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2

Heterozygous Deletions in MKRN3 Cause Central Precocious Pu..:

Meader, Brooke N ; Albano, Alessandro ; Sekizkardes, Hilal.
The Journal of Clinical Endocrinology & Metabolism.  105 (2020)  8 - p. 2732-2739 , 2020
 
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Diagnostic Value of Anthropometric Measurements for Familia..:

Vasandani, Chandna ; Li, Xilong ; Sekizkardes, Hilal...
The Journal of Clinical Endocrinology & Metabolism.  105 (2020)  7 - p. 2132-2141 , 2020
 
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5

Clinical and laboratory characteristics and follow up of 62..:

Kaplowitz, Paul ; Sekizkardes, Hilal
International Journal of Pediatric Endocrinology.  2019 (2019)  1 - p. , 2019
 
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MON-159 Increased Gluconeogenesis and Lower Glycogenolysis ..:

Sekizkardes, Hilal ; Chung, Stephanie ; Chacko, Shaji...
Journal of the Endocrine Society.  3 (2019)  Supplement_1 - p. , 2019
 
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Efficacy of Metreleptin Treatment in Familial Partial Lipod..:

Sekizkardes, Hilal ; Cochran, Elaine ; Malandrino, Noemi..
The Journal of Clinical Endocrinology & Metabolism.  104 (2019)  8 - p. 3068-3076 , 2019
 
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Thyroid Hormone Effects on Glucose Disposal in Patients Wit..:

Kushchayeva, Yevgeniya S ; Startzell, Megan ; Cochran, Elaine...
The Journal of Clinical Endocrinology & Metabolism.  105 (2019)  3 - p. e158-e171 , 2019
 
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11

Phenotypic differences among Familial Partial Lipodystrophy..:

Vasandani, Chandna ; Li, Xilong ; Sekizkardes, Hilal..
Vasandani C, Li X, Sekizkardes H, Brown RJ, Garg A. Data from: Phenotypic differences among familial partial lipodystrophy due to LMNA or PPARG variants. UT Southwestern Institutional Repository 2022. Deposited 5 August 2022. https://hdl.handle.net/2152.5/9949.  , 2022
 
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