Chwilio eraill:
family disease » familial disease (Ehangu'r Chwiliad), early disease (Ehangu'r Chwiliad)
central nerve » ventral nerve (Ehangu'r Chwiliad), central nervous (Ehangu'r Chwiliad), central neural (Ehangu'r Chwiliad)
nerve family » nerve fails (Ehangu'r Chwiliad), service family (Ehangu'r Chwiliad), nervosa family (Ehangu'r Chwiliad)
celia serve » celia herve (Ehangu'r Chwiliad), celik servet (Ehangu'r Chwiliad), cells serve (Ehangu'r Chwiliad)
benet nerve » bent nerve (Ehangu'r Chwiliad), detect nerve (Ehangu'r Chwiliad), benign nerve (Ehangu'r Chwiliad)
nerve cyst » nerve cystic (Ehangu'r Chwiliad), nerve case (Ehangu'r Chwiliad), nerve cat (Ehangu'r Chwiliad)
i central » coli central (Ehangu'r Chwiliad), hemi central (Ehangu'r Chwiliad)
a celia » a celiac (Ehangu'r Chwiliad), ma celia (Ehangu'r Chwiliad), a celik (Ehangu'r Chwiliad)
serve a » serve _ (Ehangu'r Chwiliad), reserve a (Ehangu'r Chwiliad)
j benet » j bennett (Ehangu'r Chwiliad), j benito (Ehangu'r Chwiliad), j benesi (Ehangu'r Chwiliad)
a dis » a dos (Ehangu'r Chwiliad), a des (Ehangu'r Chwiliad), a dia (Ehangu'r Chwiliad)
Dangos 1 - 20 canlyniadau o 162 ar gyfer chwilio '(((( a celia serve a dis ) OR ( i central nerve family disease ))) OR ( j benet nerve cyst due ))*', amser ymholiad: 1.91e Mireinio'r Canlyniadau
rPbPga1 from Paracoccidioides brasiliensis Activates Mast Cells and Macrophages via NFkB
Analysis of autosomal dominant spinocerebellar ataxia type 1 in an extended family of central India

Differential expression of neuregulin-1 isoforms and downregulation of erbin are associated with Erb B2 receptor activation in diabetic peripheral neuropathy
Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease

Hereditary motor and sensory neuropathy, caused by mutations in the NEFL gene in a family from Karachaevo-Cherkessia
Hereditary sensory neuropathy type I

Non-Type I Cystinuria Associated with Mental retardation and Ataxia in a Korean Boy with a New Missence Mutation(G173R) in the SLC7A9 Gene
ATP Receptors Gate Microglia Signaling in Neuropathic Pain

Risk of Herpes Zoster and Family History: A Meta-analysis of Case-control Studies
Diagnostic laboratory testing for Charcot Marie Tooth disease (CMT): the spectrum of gene defects in Norwegian patients with CMT and its implications for future genetic test strategies

A Novel Missense Mutation in AIFM1 Results in Axonal Polyneuropathy and Misassembly of OXPHOS Complexes
Re-engineering of the damaged brain and spinal cord evidence-based neurorehabilitation /

Cytoskeleton of the nervous system
Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature

Immediate early genes in sensory processing, cognitive performance and neurological disorders
The Assessment of Oropharyngeal Dysphagia in Adults

A LRSAM1 mutation links Charcot–Marie–Tooth type 2 to Parkinson's disease
The change of HCN1/HCN2 mRNA expression in peripheral nerve after chronic constriction injury induced neuropathy followed by pulsed electromagnetic field therapy

Presence of Fleischer ring and prominent corneal nerves in keratoconus relatives and normal controls
Progressive optic nerve changes in cavitary optic disc anomaly: integration of copy number alteration and cis-expression quantitative trait loci to assess disease etiology

Offerynnau Chwilio: Cael Porthiant RSS — E-bostio'r Chwiliad hwn — Cadw'r Chwiliad