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1 . Academic Journal
Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy
저자
by
Shamita Sanga
;
Sudipta Chakraborty
;
Mainak Bardhan
;
Kiran Polavarapu
;
Veeramani Preethish Kumar
, et al.
소스
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Open Access (DOAJ)
Web of Science
Scopus
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7 . Academic Journal
Infantile spasms: Etiology, lead time and treatment response in a resource limited setting
저자
by
Priyanka Surana
;
Joseph D. Symonds
;
Prabhar Srivastava
;
Thenral S. Geetha
;
Romit Jain
, et al.
소스
Epilepsy & Behavior Reports, Vol 14, Iss , Pp 100397- (2020)
Full Text (ScienceDirect)
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7 .
Identification of a shared, common haplotype segregating with an SGCB c.544T>G mutation in Indian patients affected with sarcoglycanopathy
저자
by
Shamita Sanga
;
Sudipta Chakraborty
;
Mainak Bardhan
;
Kiran Polavarapu
;
Veeramani Preethish Kumar
, et al.
소스
Open Access (OpenAIRE)
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7 .
Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A > C
저자
by
Mainak Bardhan
;
Ram Murthy Anjanappa
;
Kiran Polavarapu
;
Veeramani Preethish-Kumar
;
Seena Vengalil
, et al.
소스
neurogenetics
. 23:187-202
Web of Science
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7 .
Oculogyric Crisis Phenotype of Levodopa‐Induced Ocular Dyskinesia
저자
by
Diana A. Olszewska
;
Rajesh Shetty
;
Thenral S. Geetha
;
Vedam L. Ramprasad
;
Anthony E. Lang
, et al.
소스
Mov Disord Clin Pract
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7 .
Genotype-phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India
저자
by
Saraswati Nashi
;
Kiran Polavarapu
;
Mainak Bardhan
;
Ram Murthy Anjanappa
;
Veeramani Preethish-Kumar
, et al.
소스
Neurogenetics
.
Scopus
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7 .
Clinical Study of 668 Indian Subjects with Juvenile, Young, and Early Onset Parkinson’s Disease
저자
by
Rupam Borgohain
;
Shymal K Das
;
Hrishikesh Kumar
;
Pettarusp M Wadia
;
Soaham Desai
, et al.
소스
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
. 49:93-101
Web of Science
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7 .
Metabolic and Genetic Evaluation in Children with Nephrolithiasis
저자
by
Anita Mandal
;
Priyanka Khandelwal
;
Thenral S. Geetha
;
Sakthivel Murugan
;
Jitendra Meena
, et al.
소스
Indian journal of pediatrics
. 89(12)
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7 .
A Case of Autosomal Dominant Ataxia with Vocal Cord Palsy Attributed to a Mutation in the
PRNP
Gene
저자
by
Vedam L. Ramprasad
;
Anita Mahadevan
;
Thenral S. Geetha
;
Prashanth L. Kukkle
.
소스
Mov Disord Clin Pract
Open Access (OpenAIRE)
Web of Science
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6 .
A Rare Neurological Presentation of Familial Hemophagocytic Lymphohistiocytosis
저자
by
Vedam L. Ramprasad
;
Mukesh Desai
;
Omkar Hajirnis
;
Tarishi Nemani
;
Ritu Kashikar
, et al.
소스
Journal of Pediatric Neurology
. 19:092-101
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