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Kayihan Uluc

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Journal of the Neurological Sciences|July 16, 2008

Leukoencephalopathy with brain stem and spinal cord involvement and high lactate: a genetically proven case with distinct MRI findingsKayihan Uluc, Ozdil Baskan, Kadriye Agan Yildirim, et al.

Neurology. Genetics|January 31, 2018

Homozygous <i>CAPN1</i> mutations causing a spastic-ataxia phenotype in 2 familiesCemile Kocoglu, Asli Gundogdu, Gulsen Kocaman, et al.

Human Genetics|April 21, 2015

Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysisDavut Pehlivan, Zeynep Coban Akdemir, Ender Karaca, et al.

Journal of the Peripheral Nervous System : JPNS|January 31, 2024

Electrodiagnostic methods to verify Guillain-Barré syndrome subtypes in Istanbul: A prospective multicenter studyVolkan Tasdemir, Nermin Gorkem Sirin, Arman Cakar, et al.

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Search research articles

Showing results (31-40 of 34) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 34 results.

Journal of the Neurological Sciences|July 16, 2008

Leukoencephalopathy with brain stem and spinal cord involvement and high lactate: a genetically proven case with distinct MRI findingsKayihan Uluc, Ozdil Baskan, Kadriye Agan Yildirim, et al.

Neurology. Genetics|January 31, 2018

Homozygous <i>CAPN1</i> mutations causing a spastic-ataxia phenotype in 2 familiesCemile Kocoglu, Asli Gundogdu, Gulsen Kocaman, et al.

Human Genetics|April 21, 2015

Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysisDavut Pehlivan, Zeynep Coban Akdemir, Ender Karaca, et al.

Journal of the Peripheral Nervous System : JPNS|January 31, 2024

Electrodiagnostic methods to verify Guillain-Barré syndrome subtypes in Istanbul: A prospective multicenter studyVolkan Tasdemir, Nermin Gorkem Sirin, Arman Cakar, et al.

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