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Arya, Sneha
80  results:
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1

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

Phadte, Aditya ; Dhole, Charushila ; Hegishte, Samiksha...
Clinical Endocrinology.  100 (2024)  5 - p. 431-440 , 2024
Link: https://doi.org/10.1111/..
 
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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/..
 
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3

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/..
 
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4

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/..
 
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5

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/..
 
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6

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/..
 
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7

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/..
 
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8

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/..
 
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9

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/..
 
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10

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/..
 
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11

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/..
 
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12

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/..
 
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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/..
 
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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/..
 
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15

Expanding genetic spectrum and discriminatory role of stero..:

Karlekar, Manjiri Pramod ; Sarathi, Vijaya ; Lila, Anurag...
Clinical Endocrinology.  94 (2020)  4 - p. 533-543 , 2020
Link: https://doi.org/10.1111/..
 
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