Hereditary Motor Syndromes
Mitotoxicity in distal symmetrical sensory peripheral neuropathies | Nature Reviews Neurology
Hereditary neuropathies | PPT
Peripheral Neuropathy Made Easy | Epomedicine
Venn diagram of disease genes for Charcot-Marie-Tooth disease... | Download Scientific Diagram
Distal hereditary motor neuropathies (dHMN) | SpringerLink
Diagnosis of peripheral neuropathy | Neurological Research and Practice | Full Text
Distal hereditary motor neuropathy with vocal cord paresis: from difficulty in choral singing to a molecular genetic diagnosis | Practical Neurology
Confirmation of SLC5A7‐related distal hereditary motor neuropathy 7 in a family outside Wales - Hamanaka - 2018 - Clinical Genetics - Wiley Online Library
Altered TDP‐43‐dependent splicing in HSPB8‐related distal hereditary motor neuropathy and myofibrillar myopathy - Cortese - 2018 - European Journal of Neurology - Wiley Online Library
Autosomal Recessive Distal Hereditary Motor Neuropathy disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Distal hereditary motor neuropathy, type II: MedlinePlus Genetics
Distal Hereditary Motor Neuronopathy Type 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
A family with distal hereditary motor neuropathy and a K141Q mutation of small heat shock protein HSPB1. | Semantic Scholar
Peripheral neuropathy - The Lancet
Variants in MME are associated with autosomal‐recessive distal hered
Charcot-Marie-Tooth Neuropathy with Pyramidal Features | SpringerLink
Diabetic Neuropathies - Endotext - NCBI Bookshelf
Frontiers | Clinical and Genetic Features of Biallelic Mutations in SORD in a Series of Chinese Patients With Charcot-Marie-Tooth and Distal Hereditary Motor Neuropathy
The given table describes the different types of Distal Hereditary... | Download Scientific Diagram
Figure 2 from A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy | Semantic Scholar
Clinical heterogeneity of different forms of hereditary motor... | Download Scientific Diagram
Hereditary Neuropathy Foundation - Could you be 1 of the estimated 3300 patients in the US with the gene causing SORD Deficiency? You may have been diagnosed with CMT2, or distal hereditary
Distal hereditary motor neuropathy type V - Know It ALL 🔊✓ - YouTube
Peripheral Neuropathy: More Than a (Loss of) Feeling
Variable phenotypic expression and onset in MYH14 distal hereditary motor neuropathy phenotype in a large, multigenerational North American family. - Abstract - Europe PMC
