[Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy]

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

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology·2008

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

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology·2006

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

Neurology·2006

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

Neuropediatrics·2005

A novel MPZ gene mutation in congenital neuropathy with hypomyelination.

Neurology·2004

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

Neuromuscular disorders : NMD·2004

Cerebral infarcts in newborns and infants with cyanotic cardiac anomalies.

Neuropatologia polska·1993

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

Neuropatologia polska·1993

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

Neuropatologia polska·1993

Paraneoplastic subacute sensory neuronopathy. Clinical-pathological study.

Neuropatologia polska·1993

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

Neuroprotection of engineered Clostridium butyricum-pMTL007-GLP-1 in A53T α-synuclein (α-syn) mouse model via PI3K/AKT/GSK-3β.

Journal of Zhejiang University. Science. B·2026

Incidence and clinical characteristics of amyotrophic lateral sclerosis during the post-COVID-19 Period: a population-based study from Isfahan, Iran.

Neurodegenerative disease management·2026

Extragonadal Seminoma: Simultaneous Involvement of the Anterior Mediastinum and Central Nervous System.

Cureus·2026

Tracing neuroinflammation in neurodegeneration: insights from a scoping review on biofluid biomarkers.

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Three Cases of Primary Central Airway Tumors of Neurological and Neuroendocrine Origin in Children.

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Related Experiment Videos

[Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy]

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.

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

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.

Rare coexistence of congenital malformations in adult.

Neuroprotection of engineered Clostridium butyricum-pMTL007-GLP-1 in A53T α-synuclein (α-syn) mouse model via PI3K/AKT/GSK-3β.

Incidence and clinical characteristics of amyotrophic lateral sclerosis during the post-COVID-19 Period: a population-based study from Isfahan, Iran.

Extragonadal Seminoma: Simultaneous Involvement of the Anterior Mediastinum and Central Nervous System.

Tracing neuroinflammation in neurodegeneration: insights from a scoping review on biofluid biomarkers.

Three Cases of Primary Central Airway Tumors of Neurological and Neuroendocrine Origin in Children.

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[Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy]

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