Keywords: ANN; Artificial Neural Network; CA, CB, CC, CD; Combination A, B, C, D; DO; dissolved oxygen; EC; electrical conductivity; GRNN; General Regression Neural Network; hydro PP; hydro power plant; HNPP; Hungarian Nuclear Power Plant; IA; Willmott's index of
مقالات ISI (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: Nervensonographie; MR-Neurographie; hereditäre Neuropathien; CIDP; ALS; Nerve ultrasound; magnetic resonance neurography; hereditary neuropathies; CIDP; amyotrophic lateral sclerosis; ALS; Amyotrophe Lateralsklerose; CIDP; Chronisch Demyelinisierende Inf
Keywords: Mononeuropathies; HNPP; Childhood; Hereditary; PMP22 protein
Keywords: Action potential; Nerve conduction study; Sensory nerve action potential; Compound muscle action potential; Ion channel; Voltage-gated sodium channel; Voltage-gated potassium channel; Node of Ranvier; Paranode; Juxtaparanode; Septate-like junction; Tight
Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo
Keywords: CMT; Charcot-Marie-Tooth disease; siRNA; small interfering RNA; PMP22; peripheral myelin protein 22Â kD; MBP; myelin basic protein; MPZ; myelin protein zero; IPN; Inherited peripheral neuropathy; HMSN; hereditary motor and sensory neuropathy; HNPP; heredi
Skin biopsy and microneurography disclose selective noradrenergic dysfunction due to dopamine-β-hydroxylase deficiency
Keywords: DβH; dopamine-β-hydroxylase; PAN; peripheral autonomic neuropathy; OH; orthostatic hypotension; HNPP; hereditary neuropathy with liability to pressure palsies; MSNA; muscle sympathetic nerve activity; SSNA; skin sympathetic nerve activity; PGP 9.5; gene
The shifting paradigm of Charcot-Marie-Tooth disease
Keywords: Charcot-Marie-Tooth disease; Hereditary polyneuropathy; Maladie de Charcot-Marie-Tooth; Polyneuropathie héréditaire; AD; autosomal dominant; AR; autosomal recessive; CMT; Charcot-Marie-Tooth disease; CMT1; autosomal dominant demyelinating CMT; CMT2; aut
Transient expression of neuropeptide W in postnatal mouse hypothalamus - A putative regulator of energy homeostasis
Keywords: AgRP; Agouti-related protein; ARC; arcuate nucleus; CART; cocaine amphetamine-regulated transcript; DA; dopamine; DMH; dorsomedial hypothalamus; GABA; gamma-aminobutyric acid; HNPP; 2-hydroxy-3-naphtoic acid-2â²-phenylanilide phosphate; IgG; immunoglobul
Peripheral Myelin Protein 22 gene duplication with atypical presentations: A new example of the wide spectrum of Charcot-Marie-Tooth 1A disease
Keywords: Charcot-Marie-Tooth disease; CMT1A; HNPP; PMP22; Tomacula;
Variable phenotypes are associated with PMP22 missense mutations
Keywords: Charcot-Marie-Tooth disease; PMP22; HNPP
A case of rare recessive oculopharyngeal muscular dystrophy (OPMD) coexisting with hereditary neuropathy with liability to pressure palsies (HNPP)
Keywords: Recessive OPMD; HNPP; Inherited neuropathy; Ptosis; Dysphagia; Trinucleotide repeat
Ciliary neurotrophic factor null alleles are not a risk factor for Charcot-Marie-Tooth disease, hereditary neuropathy with pressure palsies and amyotrophic lateral sclerosis
Keywords: CMT; Charcot-Marie-Tooth disease; HNPP; hereditary neuropathy with pressure palsies; ALS; amyotrophic lateral sclerosis; CNTF; Null allele; CMT; HNPP; ALS;
A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies
Keywords: HNPP; PMP22 gene; Frameshift mutation
A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsies
Keywords: HNPP; PMP22 gene; Frameshift mutation;
Co-segregation of LMNA and PMP22 gene mutations in the same family
Keywords: LGMD1B; HNPP; LMNA; PMP22;
The Prevalence of Hereditary Neuropathy With Liability to Pressure Palsies in Patients With Multiple Surgically Treated Entrapment Neuropathies
Keywords: HNPP; carpal tunnel release; ulnar nerve transposition; entrapment neuropathy;
Ionizing radiation and genetic risks
Keywords: AS; Angelman syndrome; BEIR Committee; Biological Effects of Ionizing Radiation committee of the U.S. National Academy of Sciences; BFB; Breakage fusion bridge cycle; CMT1A; Charcot-Marie-Tooth disease type 1A; DGS/VCFS; Di George/Velocardiofacial syndrom