Pesquisas alternativas:
absent nerve » bent nerve (Expandir a Pesquisa), abducent nerve (Expandir a Pesquisa), augment nerve (Expandir a Pesquisa)
crest nerve » treat nerve (Expandir a Pesquisa), crest derived (Expandir a Pesquisa), current nerve (Expandir a Pesquisa)
j absent » _ absent (Expandir a Pesquisa), 1 absent (Expandir a Pesquisa), l absent (Expandir a Pesquisa)
i crest » i crestr (Expandir a Pesquisa), _ crest (Expandir a Pesquisa), a crest (Expandir a Pesquisa)
van die » van dijk (Expandir a Pesquisa)
case di » case did (Expandir a Pesquisa), case dti (Expandir a Pesquisa), case de (Expandir a Pesquisa)
van de » van der (Expandir a Pesquisa), van den (Expandir a Pesquisa)
case d » case de (Expandir a Pesquisa), case 1 (Expandir a Pesquisa), case 2 (Expandir a Pesquisa)
A mostrar 1 - 20 resultados de 39 para a pesquisa '(( i crest nerve ((van die) OR (van de)) ) OR ( j absent nerve ((case di) OR (case d)) ))*', tempo de pesquisa: 3.18seg Refinar resultados
Carcinosarcoma of the parotid gland with mucoepidermoid carcinoma component
Distribution and Development of Peripheral Glial Cells in the Human Fetal Cochlea

Anomalous Facial Nerve Canal with Cochlear Malformations
Atrophy of the Posterior Cricoarytenoid Muscle as an Indicator of Recurrent Laryngeal Nerve Palsy

Sensory neuropathy as part of the cerebellar ataxia neuropathy vestibular areflexia syndrome
Declaring pediatric brain death: current practice in a Canadian pediatric critical care unit.

E-ABR in Patients with Cochlear Implant: A Comparison between Patients with Malformed Cochlea and Normal Cochlea
Calcium dependence of damage to mouse motor nerve terminals following oxygen/glucose deprivation

Enhanced B7 costimulatory molecule expression in inflammatory human sural nerve biopsies
Human Melanoma Initiating Cells Express Neural Crest Nerve Growth Factor Receptor CD271

Intraoperative Electrocochleographic Characteristics of Auditory Neuropathy Spectrum Disorder in Cochlear Implant Subjects
Congenital Myasthenic Syndrome - A Report Of Nineteen Cases

Target-enrichment sequencing and copy number evaluation in inherited polyneuropathy
Critical illness myopathy after COVID-19

Presynaptic imidazoline receptors and non-adrenoceptor[(3)H]-idazoxan binding sites in human cardiovascular tissues
The effects of stimulating cutaneous and splanchnic afferents on cerebellar unit discharges

Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment
Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment

Autosomal recessive hereditary motor and sensory neuropathy with mental retardation, optic atrophy and pyramidal signs.
Locomotion-related variations in excitability of spino-olivocerebellar paths to cat cerebellar cortical c2 zone.

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