Tarkoititko:
current nerve » recurrent nerve (Laajenna hakua), current service (Laajenna hakua), current energy (Laajenna hakua)
absent nerve » bent nerve (Laajenna hakua), abducent nerve (Laajenna hakua), augment nerve (Laajenna hakua)
nerve caused » nerve case (Laajenna hakua), nerve based (Laajenna hakua), nerve crush (Laajenna hakua)
renal nerve » retinal nerve (Laajenna hakua), cranial nerve (Laajenna hakua), spinal nerve (Laajenna hakua)
nerve cnase » nerve case (Laajenna hakua), nerve cases (Laajenna hakua), nerve cause (Laajenna hakua)
caused de » caused due (Laajenna hakua), caused deep (Laajenna hakua), caused dose (Laajenna hakua)
nerve cn » nerve can (Laajenna hakua), nerve c (Laajenna hakua), nerve co (Laajenna hakua)
_ absent » _ absence (Laajenna hakua)
cn diet » can diet (Laajenna hakua), 6n diet (Laajenna hakua), n diet (Laajenna hakua)
j renal » j real (Laajenna hakua), j renaldi (Laajenna hakua), j renata (Laajenna hakua)
cnase d » chase d (Laajenna hakua), case d (Laajenna hakua), rnase d (Laajenna hakua)
Näytetään 1 - 20 yhteensä 21 tuloksesta haulle '(( 19 current nerve cn diet ) OR ((( _ absent nerve caused de ) OR ( j renal nerve cnase d ))))*', hakuaika: 2,01s Tarkenna hakua
Unilateral Idiopathic Sensory Trigeminal Nerve Paralysis in a Dog
A rare case of concomitant sicca keratopathy and ipsilateral central facial palsy in Wallenberg’s dorsolateral medullary syndrome

Type 1 ryanodine receptor knock-in mutation causing central core disease of skeletal muscle also displays a neuronal phenotype
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination

X-linked spinal and bulbar muscular atrophy (Kennedy's disease) with long-term electrophysiological evaluation: case report Atrofia muscular bulbo-espinal ligada ao cromossomo X (doença de Kennedy) com seguimento eletrofisiológico de longo prazo: relato de caso
Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

Sites of action of Mojave toxin isolated from the venom of the Mojave rattlesnake
Teneurin-4 Is a Novel Regulator of Oligodendrocyte Differentiation and Myelination of Small-Diameter Axons in the CNS

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders
Recurrent De Novo Mutations Disturbing the GTP/GDP Binding Pocket of RAB11B Cause Intellectual Disability and a Distinctive Brain Phenotype

Novel Mutation in CNTNAP1 results in Congenital Hypomyelinating Neuropathy
Optic Nerve Hypoplasia Syndrome: A Review of the Epidemiology and Clinical Associations

Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel RAB7A Mutation and Inhibited EGFR Degradation
Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel <i>RAB7A</i> Mutation and Inhibited EGFR Degradation

A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvement
A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3

Histomorphometric and sympathetic innervation of the human superficial temporal artery
Antibodies to neurofascin, contactin-1, and contactin-associated protein 1 in CIDP: Clinical relevance of IgG isotype

Novel expression pattern of neuropeptide Y immunoreactivity in the peripheral nervous system in a rat model of neuropathic pain
Evaluation of agreement between tests for the diagnosis of leprosy

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