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Gowda, Vykuntaraju K
177  Ergebnisse:
Personensuche X
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1

KCTD7‐related progressive myoclonic epilepsy: Report of 42 ..:

Yoganathan, Sangeetha ; Whitney, Robyn ; Thomas, Maya...
Epilepsia.  65 (2024)  3 - p. 709-724 , 2024
Link: https://doi.org/10.1111/..
 
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2

Lack of association of Stevens–Johnson syndrome/toxic epide..:

Srinivas, Sahana M. ; Gowda, Vykuntaraju K. ; Gowdra, Aruna..
International Journal of Dermatology.  63 (2024)  5 - p. , 2024
Link: https://doi.org/10.1111/..
 
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3

Diagnostic markers of acute encephalitis syndrome and COVID..:

Damodar, Tina ; Dunai, Cordelia ; Prabhu, Namratha...
Journal of Medical Virology.  96 (2024)  5 - p. , 2024
Link: https://doi.org/10.1002/..
 
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4

Molybdenum Cofactor Deficiency (MoCD) Masquerading as Strok..:

Gowda, Vykuntaraju K. ; Markose, Annsmol P. ; Reddy, Viveka Santhosh.
Indian Journal of Pediatrics.  91 (2024)  7 - p. 757-757 , 2024
Link: https://doi.org/10.1007/..
 
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5

Midfacial toddler excoriation syndrome (MiTES): case series..:

Sarveswaran, Nivedita ; Pamela, Yunisa ; Reddy, Akhila A N...
British Journal of Dermatology.  , 2024
Link: https://doi.org/10.1093/..
 
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6

Amyotrophic Lateral Sclerosis due to ALS2 Pathogenic Varian..:

Gowda, Vykuntaraju K. ; Babu, Sharath ; Kinhal, Uddhava.
Indian Journal of Pediatrics.  91 (2024)  8 - p. 872-872 , 2024
Link: https://doi.org/10.1007/..
 
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7

Comprehensive immunoprofiling of neurodevelopmental disorde..:

Sreenivas, Nikhitha ; Maes, Michael ; Padmanabha, Hansashree...
Brain, Behavior, and Immunity.  115 (2024)  - p. 505-516 , 2024
Link: https://doi.org/10.1016/..
 
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8

Rare Treatable Neurometabolic Condition — Adenosine Kinase ..:

Gowda, Vykuntaraju K. ; Babu, Sharath ; Kinhal, Uddhava.
Indian Journal of Pediatrics.  , 2024
Link: https://doi.org/10.1007/..
 
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9

Amyotrophic Lateral Sclerosis due to ALS2 Pathogenic Varian..:

Gowda, Vykuntaraju K. ; Babu, Sharath ; Kinhal, Uddhava.
Indian Journal of Pediatrics.  , 2024
Link: https://doi.org/10.1007/..
 
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10

Refining the phenotype of SINO syndrome: A comprehensive co..:

Alstrup, Morten ; Cesca, Fabrizia ; Krawczun-Rygmaczewska, Alicja...
Genetics in Medicine.  , 2024
Link: https://doi.org/10.1016/..
 
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11

In silico characterization and identification of compound h..:

Gowda, Vykuntaraju K. ; Srinivasan, Varunvenkat M. ; Srivastava, Sudhanshu...
Journal of Family Medicine and Primary Care.  13 (2024)  1 - p. 208-220 , 2024
Link: https://doi.org/10.4103/..
 
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12

Genetically Confirmed Case of Aspartylglycosaminuria (AGU):

Gowda, Vykuntaraju K. ; Khemalapures, Ruchita ; Kinhal, Uddhava.
Indian Journal of Pediatrics.  , 2024
Link: https://doi.org/10.1007/..
 
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13

Clinical and Molecular Spectrum of Autosomal Recessive CA8‐..:

Kaiyrzhanov, Rauan ; Ortigoza‐Escobar, Juan Darío ; Stringer, Brett W....
Movement Disorders.  39 (2024)  6 - p. 983-995 , 2024
Link: https://doi.org/10.1002/..
 
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14

Development, validation and application of single molecule ..:

Sheth, Harsh ; Nair, Aadhira ; Bhavsar, Riddhi...
Human Genomics.  18 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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15

L-Serine Biosynthesis Defect: A Treatable Condition Masquer..:

Gowda, Vykuntaraju K. ; Roy, Amaresh ; Kinhal, Uddhava.
Indian Journal of Pediatrics.  , 2024
Link: https://doi.org/10.1007/..
 
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