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Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 gene.

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Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene.

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Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 gene.

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A novel MPZ gene mutation in congenital neuropathy with hypomyelination.

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A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin.

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Cerebral infarcts in newborns and infants with cyanotic cardiac anomalies.

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Effect of clinical death on inositol 1,4,5-trisphosphate in the rat brain.

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Intravascular coagulation in the central nervous system in patients with acute myeloblastic leukemias.

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Morphological changes in the peripheral nervous system in the case of congenital malformations of the spinal cord.

Neuropatologia polska·1993

Rare coexistence of congenital malformations in adult.

Neuropatologia polska·1993

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Naphthoquinones mediate differentiation of human umbilical cord derived mesenchymal stem cells into insulin producing cells through regulation of Wnt and BMP pathways.

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Prevalence of Probable REM Sleep Behavior Disorder in Essential Tremor.

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[Histological changes in the ulnar and sural nerves in amyotrophic lateral sclerosis]

Related Concept Videos

Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 gene.

Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 gene.

Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene.

Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 gene.

A novel MPZ gene mutation in congenital neuropathy with hypomyelination.

A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin.

Cerebral infarcts in newborns and infants with cyanotic cardiac anomalies.

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Intravascular coagulation in the central nervous system in patients with acute myeloblastic leukemias.

Paraneoplastic subacute sensory neuronopathy. Clinical-pathological study.

Morphological changes in the peripheral nervous system in the case of congenital malformations of the spinal cord.

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Nanotechnology-enabled delivery of bioactive compounds for neuroprotection in Parkinson's disease: mechanisms and future directions.

Diabetic striatopathy and concurrent peri-ictal cortical diffusion restriction in nonketotic hyperglycemia: A rare stroke mimic.

Neurogenic gastrointestinal, urinary, and sexual dysfunction in multiple sclerosis: a multidisciplinary framework for clinical practice.

Naphthoquinones mediate differentiation of human umbilical cord derived mesenchymal stem cells into insulin producing cells through regulation of Wnt and BMP pathways.

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