E-LIB Suche - Ergebnisse für: Arya, Sneha

1

Steroidogenic acute regulatory protein (STAR) deficiency: O..:

Phadte, Aditya ; Dhole, Charushila ; Hegishte, Samiksha...
Clinical Endocrinology. 100 (2024) 5 - p. 431-440 , 2024

2

46,XX aromatase deficiency: A single-center experience with..:

Yami channaiah, Chethan ; Memon, Saba Samad ; Sarathi, Vijaya...
Annales d'Endocrinologie. 85 (2024) 1 - p. 48-55 , 2024

Link: https://doi.org/10.1016/..

3

Genotypic Spectrum and its Correlation with Alopecia and Cl..:

Dodamani, Manjunath Havalappa ; Lila, Anurag Ranjan ; Memon, Saba Samad...
Calcified Tissue International. 112 (2023) 4 - p. 483-492 , 2023

Link: https://doi.org/10.1007/..

4

Hereditary Hypophosphatemic Rickets with Hypercalciuria Pre..:

Dodamani, Manjunath Havalappa ; Memon, Saba Samad ; Karlekar, Manjiri...
Calcified Tissue International. 114 (2023) 2 - p. 137-146 , 2023

Link: https://doi.org/10.1007/..

5

Regional genotypic variations in normosmic congenital hypog..:

Patil, Virendra A. ; Lila, Anurag Ranjan ; Shah, Nalini...
Pituitary. 25 (2022) 3 - p. 444-453 , 2022

Link: https://doi.org/10.1007/..

6

17β hydroxysteroid dehydrogenase 3 deficiency in 46,XY diso..:

Krishnappa, Brijesh ; Arya, Sneha ; Lila, Anurag R....
Clinical Endocrinology. 97 (2022) 1 - p. 43-51 , 2022

Link: https://doi.org/10.1111/..

7

Pituitary stalk interruption syndrome: phenotype, predictor..:

Diwaker, Chakra ; Thadani, Puja ; Memon, Saba Samad...
Pituitary. 25 (2022) 4 - p. 645-652 , 2022

Link: https://doi.org/10.1007/..

8

Side‐chain cleavage enzyme deficiency: Systematic review an..:

Phadte, Aditya ; Arya, Sneha ; Sarathi, Vijaya...
Clinical Endocrinology. 98 (2022) 3 - p. 351-362 , 2022

Link: https://doi.org/10.1111/..

9

Genotype–Phenotype Correlations in Asian Indian Children an..:

Sharma, Anima ; Memon, Saba ; Lila, Anurag R....
Calcified Tissue International. 111 (2022) 3 - p. 229-241 , 2022

Link: https://doi.org/10.1007/..

10

Genetic spectrum of Kallmann syndrome: Single‐center experi..:

Patil, Virendra A. ; Lila, Anurag Ranjan ; Shah, Nalini...
Clinical Endocrinology. 97 (2022) 6 - p. 804-813 , 2022

Link: https://doi.org/10.1111/..

11

17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experi..:

Maheshwari, Madhur ; Arya, Sneha ; Lila, Anurag Ranjan...
Journal of the Endocrine Society. 6 (2022) 3 - p. , 2022

Link: https://doi.org/10.1210/..

12

Luteinizing hormone β‐subunit deficiency: Report of a novel..:

Barnabas, Rohit ; Jadhav, SwatiRamteke ; Arya, Sneha...
Clinical Endocrinology. 98 (2022) 3 - p. 383-393 , 2022

Link: https://doi.org/10.1111/..

13

POU1F1 mutations in combined pituitary hormone deficiency: ..:

Jadhav, Swati ; Diwaker, Chakra ; Lila, Anurag R....
Pituitary. 24 (2021) 5 - p. 657-669 , 2021

Link: https://doi.org/10.1007/..

14

Exonic WT1 pathogenic variants in 46,XY DSD associated with..:

Arya, Sneha ; Kumar, Sandeep ; Lila, Anurag R...
Endocrine Connections. 10 (2021) 12 - p. 1522-1530 , 2021

Link: https://doi.org/10.1530/..

15

Genetic spectrum and predictors of mutations in four known ..:

Kale, Shantanu ; Gada, Jugal V. ; Jadhav, Swati...
Pituitary. 23 (2020) 6 - p. 701-715 , 2020

Link: https://doi.org/10.1007/..