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Article

COLQ-Related Congenital Myasthenic Syndrome in a Child from Western India.

Neurology India - 1 Jan 2000

Pallithanam Jis J, Prabhudesai Sumant P, Naik Neeta, Gauns Shivanand

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 33642313
DOI: 10.4103/0028-3886.310105

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COLQ-Related Congenital Myasthenic Syndrome in a Child from Western India.PMID 33642313Read ↗

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COLQ-related congenital myasthenic syndrome: An integrative view.Semantic proximity Read ↗

COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrum.Semantic proximity Read ↗

Congenital myasthenic syndrome: Ten years clinical experience from a quaternary care south-Indian hospital.Semantic proximity Read ↗

Intra-familial variation in clinical manifestations and response to ephedrine in siblings with congenital myasthenic syndrome caused by novel COLQ mutations.Semantic proximity Read ↗

First Characterization of Congenital Myasthenic Syndrome Type 5 in North AfricaSemantic proximity Read ↗

Congenital long Q-T syndromes in children.Semantic proximity Read ↗

A rare mutation in the COLQ gene causing congenital myasthenic syndrome with remarkable improvement to fluoxetine: A case report.Semantic proximity Read ↗

First characterization of congenital myasthenic syndrome type 5 in North Africa.Semantic proximity Read ↗

Recurrent COLQ mutation in congenital myasthenic syndrome.Semantic proximity Read ↗

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