Results 81 to 90 of about 590 (105)

[Two new cases of X-linked intellectual developmental disorder-105 linked to a previously unreported pathogenic variant in the USP27X gene]. [PDF]

Rev Neurol
María Dolores-Sánchez C, Doval-Calvo D, Ballesta-Martínez MJ, Sánchez-Soler MJ.   +3 more
europepmc   +1 more source

[Tuberculous otitis media: A case presentation and review of european literature]. [PDF]

Rev Esp Quimioter, 2023
Aguilera-Franco M, Franco-Acosta A, Yépez-Naranjo AF, Rodríguez-Granger J, Sampedro A, Navarro-Mari JM.   +5 more
europepmc   +1 more source

[Early detection program for hearing loss at Bajio's National Medical Center]. [PDF]

Rev Med Inst Mex Seguro Soc
Olea-González AI, Del Ángel-González AJ, Chao-Pérez MP.   +2 more
europepmc   +1 more source

[Fat graft and platelet-rich plasma versus fat alone myringoplasty]. [PDF]

Rev Med Inst Mex Seguro Soc
Piñón-Hernández CD, Rico-Maldonado MÁ, Hernández-González MA, Godínez-Garcia F.   +3 more
europepmc   +1 more source

ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time. [PDF]

Genet Med
Tshering KC, DiStefano MT, Oza AM, Ajuyah P, Webb R, Edoh E, Broeren E, Ratliff J, Gitau V, Paris K, Aburyyan A, Alexander J, Albano V, Bai D, Booth KTA, Buonfiglio PI, Charfeddine C, Dalamón V, Castillo ID, Moreno-Pelayo MA, Duzkale H, Dorshorst B, Faridi R, Kenna M, Lewis MA, Luo M, Lu Y, Mkaouar R, Matsunaga T, Nara K, Pandya A, Redfield S, Roux I, Schimmenti LA, Schrauwen I, Shaaban S, Shen J, Vona B, Smith RJ, Rehm HL, Azaiez H, Abou Tayoun AN, Amr SS, ClinGen Hearing Loss Clinical Domain Working Group.   +43 more
europepmc   +1 more source

Anomalía de Jordans en síndrome de Chanarin-Dorfman. [PDF]

Adv Lab Med
Sánchez-Cortés J, Gabaldó-Barrios X.
europepmc   +1 more source

Challenges and Successes of an Audio-Technician Training Program in Guatemala. [PDF]

Semin Hear, 2020
Miller C, Harney M, Buxton C, Mallahan M.   +3 more
europepmc   +1 more source

Comment on De Rosa et al. Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America. Genes 2024, 15, 178. [PDF]

Genes (Basel)
Elgoyhen AB, Buonfiglio PI, Dalamón V.
europepmc   +1 more source

[X-linked intellectual disability syndrome with macrocephaly due to BRWD3 gene deletion]. [PDF]

Rev Neurol
Arroyo-Carrera I, Romero-Peguero R, Martín-Fernández R, Ramajo-Polo A, García-Navas Núñez V.   +4 more
europepmc   +1 more source

Epilepsy and musical perception. A perspective involving 14 patients. [PDF]

Rev Neurol
Fernández-Cabrera A, Santamaría-Montero P, García-de Soto J, Ortegón-Aguilar E, Pego-Reigosa R, López-González FJ, Rodríguez-Osorio X.   +6 more
europepmc   +1 more source