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CEDNIK Syndrome: Report of an Ultra-Rare Case from India.
Neurol India. 2021 Nov-Dec;69(6):1861-1862. doi: 10.4103/0028-3886.333502.
Neurol India. 2021.
PMID: 34979712
Free article.
No abstract available.
Prenatal Diagnosis for Primary Immunodeficiency Disorders-An Overview of the Indian Scenario.
Yadav RM, Gupta M, Dalvi A, Bargir UA, Hule G, Shabrish S, Aluri J, Kulkarni M, Kambli P, Uppuluri R, Seshadri S, Jagadeesh S, Suresh B, Raja J, Taur P, Malaischamy S, Ghosh P, Mahalingam S, Kadam P, Lashkari HP, Tamhankar P, Tamhankar V, Mithbawkar S, Bhattad S, Jhawar P, Makam A, Bansal V, Prasad M, Govindaraj G, Guhan B, Bharadwaj Tallapaka K, Desai M, Raj R, Madkaikar MR.
Yadav RM, et al.
Front Immunol. 2020 Dec 7;11:612316. doi: 10.3389/fimmu.2020.612316. eCollection 2020.
Front Immunol. 2020.
PMID: 33365035
Free PMC article.
Review.
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Clinical profile of patients with rolandic epilepsy at a clinic in rural Maharashtra.
Sable S, Sable R, Tamhankar P, Tamhankar V.
Sable S, et al.
J Family Med Prim Care. 2021 Mar;10(3):1263-1266. doi: 10.4103/jfmpc.jfmpc_1355_20. Epub 2021 Apr 8.
J Family Med Prim Care. 2021.
PMID: 34041163
Free PMC article.
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A Novel Hypomorphic CSF1R Gene Mutation in the Biallelic State Leading to Fatal Childhood Neurodegeneration.
Tamhankar PM, Zhu B, Tamhankar VP, Mithbawkar S, Seabra L, Livingston JH, Ikeuchi T, Crow YJ.
Tamhankar PM, et al. Among authors: tamhankar vp.
Neuropediatrics. 2020 Aug;51(4):302-306. doi: 10.1055/s-0040-1702161. Epub 2020 May 28.
Neuropediatrics. 2020.
PMID: 32464672
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Novel Consensus Splice Site Pathogenic Variation in THOC2 Gene Leads to Recurrent Arthrogryposis Multiplex Congenita Phenotype: A Case Report.
Tamhankar V, Tamhankar P, Chaubal R, Chaubal J, Chaubal N.
Tamhankar V, et al.
Cureus. 2021 Nov 17;13(11):e19682. doi: 10.7759/cureus.19682. eCollection 2021 Nov.
Cureus. 2021.
PMID: 34976470
Free PMC article.
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Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1.
Tamhankar PM, Vasudevan L, Kondurkar P, Niazi S, Christopher R, Solanki D, Dholakia P, Muranjan M, Kamate M, Kalane U, Sheth J, Tamhankar V, Gulati R, Vasikarla M, Danda S, Naushad SM, Girisha KM, Patil S.
Tamhankar PM, et al.
J Pediatr Genet. 2021 Sep;10(3):213-221. doi: 10.1055/s-0040-1715528. Epub 2020 Sep 2.
J Pediatr Genet. 2021.
PMID: 34504725
Free PMC article.
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Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypes.
Laugwitz L, Seibt A, Herebian D, Peralta S, Kienzle I, Buchert R, Falb R, Gauck D, Müller A, Grimmel M, Beck-Woedel S, Kern J, Daliri K, Katibeh P, Danhauser K, Leiz S, Alesi V, Baertling F, Vasco G, Steinfeld R, Wagner M, Caglayan AO, Gumus H, Burmeister M, Mayatepek E, Martinelli D, Tamhankar PM, Tamhankar V, Joset P, Steindl K, Rauch A, Bonnen PE, Froukh T, Groeschel S, Krägeloh-Mann I, Haack TB, Distelmaier F.
Laugwitz L, et al.
J Med Genet. 2022 Sep;59(9):878-887. doi: 10.1136/jmedgenet-2021-107729. Epub 2021 Oct 16.
J Med Genet. 2022.
PMID: 34656997
Free PMC article.
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