J. Gallo-Terán

发表

Elevated BMI and NT-proBNP: a potential safety predictor for community acquired pneumonia discharge from the emergency department

C. Ramos-Estebanez, P. Muñoz-Cacho, H. Alonso-Valle, 2022, European Journal of Clinical Nutrition.

Unilateral submandibular gland aplasia with ipsilateral sublingual gland hypertrophy presenting as a neck mass.

J. Gallo-Terán, B. García-Montesinos-Perea, R. Sáiz-Bustillo, 2011, Medicina oral, patologia oral y cirugia bucal.

Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF)

F. Moreno, Y. Martín, C. Morera, 2003, Human mutation.

[Auditory neuropathy due to the Q829X mutation in the gene encoding otoferlin (OTOF) in an infant screened for newborn hearing impairment].

I. del Castillo, M. Moreno-Pelayo, C. Morales-Angulo, 2006, Acta otorrinolaringologica espanola.

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.

X. Estivill, Tsutomu Suzuki, Y. Bykhovskaya, 2006, American journal of human genetics.

[Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA].

F. Moreno, I. del Castillo, M. Moreno-Pelayo, 2003, Medicina clinica.

[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].

F. Moreno, I. del Castillo, M. Villamar, 2002, Acta Otorrinolaringológica Española.

Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss

F. Moreno, Y. Martín, R. Ramírez‐Camacho, 2003, Journal of medical genetics.

The amino-terminal fragment of pro-brain natriuretic peptide in plasma as a biological marker for predicting mortality in community-acquired pneumonia: a cohort study

P. Muñoz-Cacho, H. Alonso-Valle, M. Tazón-Varela, 2016 .

Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment

J. Fernández-Luna, R. González-Aguado, A. Fontalva, 2011 .

[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 onset].

F. Moreno, I. del Castillo, M. Moreno-Pelayo, 2005, Acta otorrinolaringologica espanola.