about
Otorhinolaryngological manifestations in patients with Behçet diseaseNeurofibromatosis type 2 and its head and neck manifestations: literature review and population study in the Community of Cantabria and the province of Las PalmasHeteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss.Audio-vestibular signs and symptoms in Chiari malformation type i. Case series and literature review.Haemorrhagic lesions in oral mucosa as the presentation of idiopathic thrombocytopenic purpura.DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.Otorhinolaryngology manifestations secondary to oral sex.Horner's syndrome after neck surgery.[Ambulatory septoplasty][Diagnosis and treatment of cervical esophageal perforation in adults][Nasal sinus adenocarcinoma in patients exposed to wood dust in the Community of Cantabria, Spain][Hypoglossal nerve palsy and infectious mononucleosis][Prevalence of the 35delG mutation in the GJB2 gene, del (GJB6-D13S1830) in the GJB6 gene, Q829X in the OTOF gene and A1555G in the mitochondrial 12S rRNA gene in subjects with non-syndromic sensorineural hearing impairment of congenital/childhood oStickler and branchio-oto-renal syndromes in a patient with mutations in EYA1 and COL2A1 genes.Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF).Analysis of risk factors influencing the outcome of the Epley maneuver.[Early diagnosis of nasopharyngeal carcinoma][Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment].[Otorhinolaryngo logical manifestations in patients with Down syndrome][Etiology of severe/profound, pre/perilingual bilateral hearing loss in Cantabria (Spain)].[Prevalence of the A1555G mutation in the mitochondrial DNA in patients with cochlear or vestibular damage due to aminoglycoside-induced ototoxicity][Program of hearing loss early detection in newborn infants in Cantabria. Results of the first year of activities][Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria].[Differential diagnosis of bilateral progressive sensorineural loss. A report of a case secondary to neurofibromatosis 2]Response of head and neck epithelial cells to a DNA damage-differentiation checkpoint involving polyploidization[Simultaneous bilateral facial paralysis][Cholesterol granuloma of the petrous apex][Verrucous carcinoma of the larynx][Sphenoidal metastasis of laryngeal carcinoma][Carcinoma of the nasopharynx in Cantabria][Anaplastic carcinoma of the thyroid in a young man. A report of a case][Use of embolization in the treatment of pulsatile tinnitus secondary to dural arteriovenous fistula][Usefulness of the flexible fibroscope with working channel in the treatment of pedunculated polyps of the vocal cords][Benign cervical mesenchymoma][Major ambulatory surgery in otorhinolaryngology][Prognostic significance of DNA content measured by flow cytometry in supraglottic laryngeal carcinoma][Biopsy of the temporal artery. Experience with the use of a protocol at an ENT department][Overexpression of p53 protein in epidermoid carcinoma of the pyriform sinus][Epidemiology of Menière's disease in Cantabria]Hereditary hemorrhagic telangiectasia
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
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name
Carmelo Morales-Angulo
@ast
Carmelo Morales-Angulo
@en
Carmelo Morales-Angulo
@es
Carmelo Morales-Angulo
@nl
Carmelo Morales-Angulo
@sl
type
label
Carmelo Morales-Angulo
@ast
Carmelo Morales-Angulo
@en
Carmelo Morales-Angulo
@es
Carmelo Morales-Angulo
@nl
Carmelo Morales-Angulo
@sl
prefLabel
Carmelo Morales-Angulo
@ast
Carmelo Morales-Angulo
@en
Carmelo Morales-Angulo
@es
Carmelo Morales-Angulo
@nl
Carmelo Morales-Angulo
@sl
P106
P21
P31
P496
0000-0002-4268-2762