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论文共 96 篇作者统计合作学者相似作者

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Leigh Like Phenotype Secondary to 3-Hydroxyisobutyryl-coa Hydrolase Deficiency: A First Indian Case
Vykuntaraju K. Gowda,Varunvenkat M. Srinivasan, Viveka-Santhosh Reddy, Amena Nayyer
Karnataka paediatric journal (2024): 1-2
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Molybdenum Cofactor Deficiency (mocd) Masquerading As Stroke Like Episodes: Authors’ Reply
Vykuntaraju K. Gowda, Annsmol P. Markose, Viveka Santhosh Reddy,Varunvenkat M. Srinivasan
Indian journal of pediatrics/Indian Journal of Pediatrics (2024)
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Snijders-Blok-Campeau Syndrome (CHD3 Gene): Description of Seven Clinical Cases with Novel Pathogenic Variants
Patricia Pascual Vinagre, Jair Tenorio,Mario Cazalla,Alejandro Parra,Cristina Silvan,Natalia Gallego, Pedro Arias, Feliciano Ramos, Julian Nevado,Pablo Lapunzina, Berta Almoguera Castillo,Varunvenkat Srinivasan,Vykuntaraju K. Gowda
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 489-489
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Traumatic Brain Injury Unmasking Vitamin B12 Deficiency in an Infant with Long-Term Follow-Up
Vykuntaraju K. Gowda, Rasika T. Shankar, Viveka Santhosh Reddy Challa,Varunvenkat M. Srinivasan
Karnataka Paediatric Journal (2024): 1-3
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Expanding the Phenotype of NRROS-Related SENEBAC Syndrome
Varunvenkat M Srinivasan, Vykuntaraju K Gowda, Annsmol P Markose, Uddhava V Kinhal, Himani Pandey
American journal of medical genetics Part App.e63899-e63899, (2024)
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Rare Treatable Neurometabolic Condition — Adenosine Kinase Deficiency
Vykuntaraju K. Gowda, Sharath Babu,Uddhava Kinhal,Varunvenkat M. Srinivasan
Indian Journal of Pediatricspp.1-1, (2024)
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作者统计

#Papers: 96

#Citation: 97

H-Index: 5

G-Index: 7

Sociability: 6

Diversity: 2

Activity: 31

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