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Snehal Mallakmir

Observed name: S. Mallakmir
Observed institutions: Apollo Hospitals, Dr. Balabhai Nanavati Hospital, Surya Hospitals, Apollo Hospitals, Apollo Hospitals, Apollo Hospitals
ORCID: 0000-0001-6943-8252
Observed ORCID: 0000-0001-6943-8252
OpenAlex ID: A5035129823
Genomic Variations in ATP7B Gene in Indian Patients with Wilson Disease
2022 · Aabha Nagral, Snehal Mallakmir, et al. · The Indian Journal of Pediatrics · 12
Mutation in the Neuroblastoma Amplified Sequence Gene as a Cause of Recurrent Acute Liver Failure, Acute Kidney Injury, and Status Epilepticus
2019 · Snehal Mallakmir, Aabha Nagral, et al. · Journal of Clinical and Experimental Hepatology · 9
Herb-induced Liver Injury—A Guide to Approach. Lessons from the Tinospora cordifolia (Giloy) Case Series Story
2022 · Aabha Nagral, Omkar S. Rudra, et al. · Journal of Clinical and Experimental Hepatology · 6
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Inherited and metabolic disorders of the liver
2024 · Aabha Nagral, Snehal Mallakmir · Elsevier eBooks · 1
Multiple Sulfatase Deficiency: A Clinical Report with Neonatal Presentation
2022 · Srushti Gandhi, Snehal Mallakmir, et al. · Acta Scientific Paediatrics · 1
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A case of SMAD6 gene variant and descriptive brief insights into genetics of aortic valve disease
2025 · Snehal Mallakmir, Bhushan Chavan, et al. · Progress in Pediatric Cardiology
Co-occurrence of Phelan-McDermid syndrome and metachromatic leukodystrophy
2025 · Snehal Mallakmir, Anbukayalvizhi Chandrasekaran, et al. · International Journal of Scientific Reports
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Contributors for Volume 2
2024 · Anil Kumar Agarwal, Zahraa Al lami, et al. · Elsevier eBooks
Chromosomal Microarray on Product of Conception in Early Pregnancy Loss: A Case Report
2023 · Snehal Mallakmir, Gauri Mulgund, et al. · Apollo Medicine
A Case of Childhood Onset of Extended Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis Phenotype with Pathogenic Polymerase Gamma Variation
2023 · Ami Shah, Shilpa Kulkarni, et al. · Indian Pediatrics Case Reports
Severe Hereditary Spherocytosis Presenting with Non-Immune Fetal Hydrops
2023 · Snehal Mallakmir, Rashid Merchant, et al. · Indian Pediatrics Case Reports
A Case Report of a Child with Langerhans Cell Histiocytosis
2022 · Srushti Gandhi, Rashid Merchant, et al. · Acta Scientific Paediatrics
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MYO5B mutation causing cholestasis in the absence of Microvillous Inclusion Disease: a rare case report
2022 · Omkar Rua, Laxmi Mohanani, et al. · Journal of Clinical and Experimental Hepatology
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Lessons Learnt from A Study of Children with Duchenne Muscular Dystrophy: Approach to The Molecular Diagnosis and Its Importance in Emerging Therapies and Preventive Measures
2021 · Snehal Mallakmir, Ami Shah, et al. · Indian Journal of Genetics and Molecular Research
Lessons Learnt from a Study of Children with Duchenne Muscular Dystrophy: Approach to the Molecular Diagnosis and its Importance in Emerging Therapies and Preventive Measures
2021 · Snehal Mallakmir · Clinical Case Reports and Clinical Study
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Genetic Perspectives On Paediatric Liver Transplantation-Indications, Molecular Basis And Prognosis
2019 · Snehal Mallakmir · Gastroenterology & Hepatology Research
Osteogenesis imperfecta: an atypical association
2015 · Snehal Mallakmir, Keya Lahiri, et al. · International Journal of Research in Medical Sciences
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To study the corelation between carotid artery intima media thickness & coronary artery disease
2014 · Rohan Bhagade, Mukesh Laddha, et al. · Indian Heart Journal
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A study of peripheral arterial disease in diabetic patients in a tertiary care centre
2014 · Yuvaraj Bhosale, Mukesh Laddha, et al. · Indian Heart Journal
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Analysis of myocardial blush and ST segment recovery after revascularization for prediction of recovery of LV function
2014 · Parth Sthapak, Mukesh Laddha, et al. · Indian Heart Journal
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Works count: 20
Citation count: 29
H-index: 3
I10-index: 1
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