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publishDate:"[2010 TO 2019]"
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/vufind/Search/Results?lookfor=%22Srinivasan%2C+Varunvenkat+M%22&type=Person&filter%5B%5D=publishDate%3A%22%5B2010+TO+2019%5D%22
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PubPharm (21)
1
Bilateral Striatal Necrosis with Polyneuropathy with a Novel SLC25A19 (Mitochondrial Thiamine Pyrophosphate Carrier OMIMI*606521) Mutation : Treatable Thiamine Metabolic Disorder-A Report of Two Indian Cases
enthalten in:
Neuropediatrics
| 2019
von
Gowda, V.
|
Srinivasan, V.
|
Jehta, K.
| +1
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2
A Novel GCH1 Mutation in An Indian Child with GTP Cyclohydrolase Deficiency
enthalten in:
Indian journal of pediatrics
| 2019
von
Gowda, V.
|
Nagarajan, B.
|
Srinivasan, V.
| +1
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3
Mitochondrial Membrane Protein Associated Neurodegeneration (MPAN) with a Novel C19orf12 Mutation in the First Decade of Life
enthalten in:
Indian journal of pediatrics
| 2019
von
Gowda, V.
|
Patil, A.
|
Srinivasan, V.
| +1
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4
A Case of Juvenile Alexander Disease Presenting as Microcephaly
enthalten in:
Indian journal of pediatrics
| 2019
von
Gowda, V.
|
Srinivasan, V.
|
Jetha, K.
| +1
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5
A Case of Juvenile Alexander Disease Presenting as Microcephaly
enthalten in:
Indian journal of pediatrics
| 2019
von
Gowda, V.
|
Srinivasan, V.
|
Jetha, K.
| +1
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6
Mitochondrial Membrane Protein Associated Neurodegeneration (MPAN) with a Novel C19orf12 Mutation in the First Decade of Life
enthalten in:
Indian journal of pediatrics
| 2019
von
Gowda, V.
|
Patil, A.
|
Srinivasan, V.
| +1
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7
A Novel GCH1 Mutation in An Indian Child with GTP Cyclohydrolase Deficiency
enthalten in:
Indian journal of pediatrics
| 2019
von
Gowda, V.
|
Nagarajan, B.
|
Srinivasan, V.
| +1
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8
A Case of Juvenile Alexander Disease Presenting as Microcephaly
enthalten in:
Indian journal of pediatrics
| 2019
von
Gowda, V.
|
Srinivasan, V.
|
Jetha, K.
| +1
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9
Tay-Sachs Disease Presenting as Refractory Epilepsy with Autistic Regression Secondary to a Novel Mutation in HEXA Gene
enthalten in:
Indian journal of pediatrics
| 2018
von
Gowda, V.
|
Srinivasan, V.
|
Bhat, M.
| +1
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10
Tay-Sachs Disease Presenting as Refractory Epilepsy with Autistic Regression Secondary to a Novel Mutation in HEXA Gene
enthalten in:
Indian journal of pediatrics
| 2018
von
Gowda, V.
|
Srinivasan, V.
|
Bhat, M.
| +1
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Erscheinungsjahr: 2010-2019
Medienart
21
Aufsätze
18
E-Artikel
18
E-Ressourcen
3
Gedruckte Aufsätze
Zeitschriftentitel
17
Indian journal of pediatrics
1
Brain & development
1
Journal of pediatric neurosciences
1
Journal of tropical pediatrics
1
Neuropediatrics
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Thema
8
Case Reports
6
Journal Article
5
Letter
3
Biotin thiamine responsive basal ganglia disease
3
Dystonia
3
Neuroregression
2
C19orf12 gene
2
Globus pallidus
2
India
2
MPAN
2
Membrane Transport Proteins
2
NBIA
2
gene
1
BVVLS
1
Basal ganglia stroke
1
EC 3.2.1.52
1
EC 3.5.4.16
1
Fazio-Londe syndrome
1
GCH1 protein, human
1
GTP Cyclohydrolase
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Erscheinungszeitraum
2010-2019
8
2019
10
2018
3
2017
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Sprache
21
Englisch
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