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Search Results - Menon, Shyla R
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Spectrum of Clinical Variability with SEPT9 Gene Mutation in Hereditary Neuralgic Amyotrophy: Understanding the Pathogenesis Using Molecular Dynamics Simulation Study
by
Bhatti, Amit
,
Ravat, Sangeeta
,
Desai, Karan
,
Shekhar, Bipin R
,
Menon, Shyla R
,
Kumbhar, Bajarang V
,
Kunwar, Ambarish
,
Jain, Neeraj
,
Das, Dhanjit K
Published in
Neurology India
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Novel Mutations in Cyclin-Dependent Kinase-Like 5 (CDKL5) Gene in Indian Cases of Rett Syndrome
by
Das, Dhanjit Kumar
,
Mehta, Bhakti
,
Menon, Shyla R.
,
Raha, Sarbani
,
Udani, Vrajesh
Published in
Neuromolecular medicine
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Lenz-Majewski syndrome: Report of a case with novel mutation in PTDSS1 gene
by
Tamhankar, Parag M
,
Vasudevan, Lakshmi
,
Bansal, Vandana
,
Menon, Shyla R
,
Gawde, Harshavardhan M
,
D'Souza, Aruna
,
Babu, Shiny
,
Kondurkar, Shweta
,
Adhia, Rashmi
,
Das, Dhanjit Kumar
Published in
European journal of medical genetics
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Development and Validation of an ELISA for Hemoglobin-A2: A Novel Method for β-Thalassemia Screening in Developing Countries
by
Menon, Shyla R.
,
Khatkhatay, M. Ikram
,
Dandekar, Sucheta P.
,
Patel, Zarine M.
Published in
Journal of immunoassay & immunochemistry
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Development and Validation of an ELISA for Hemoglobin‐A 2 : A Novel Method for β‐Thalassemia Screening in Developing Countries
by
Menon, Shyla R.
,
Khatkhatay, M. Ikram
,
Dandekar, Sucheta P.
,
Patel, Zarine M.
Published in
Journal of immunoassay & immunochemistry
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Health of indigenous people: Use of health services by indigenous population can be improved
by
Devadasan, N
,
Menon, Shyla
,
Menon, Nandakumar
,
Devadasan, Roopa
Published in
BMJ
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