Results 171 to 180 of about 2,817,923 (392)

OTOMYCOSIS OF THE EXTERNAL AND THE MIDDLE EAR: CLINIC, DIAGNOSTICS AND TREATMENTS (REFERENCES REVIEW)

, 2009
E. S. Yadchenko, V. P. Sitnicov, I. D. Schlyaga   +2 more
openalex   +2 more sources

Network Representation of the External Ear [PDF]

, 1972
Mark B. Gardner, Mel S. Hawley, Mel S. Hawley   +2 more
openalex   +1 more source

Prevalence of external ear disorders in Belgian stray cats

Journal of feline medicine and surgery, 2017
Anouck Bollez, H. de Rooster, Alessandra Furcas, S. Vandenabeele   +3 more
semanticscholar   +1 more source

A Systematic Review and Meta‐Analysis of the Birth Prevalence of Turner Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Turner syndrome, a chromosomal disorder, causes short stature, pubertal arrest, amenorrhea, and infertility in females. Prevalence estimates vary widely; however, reliable estimates are important for public health initiatives. Therefore, a meta‐analysis was undertaken.
David Hinds, Jeanne M. Pimenta, Andrea Low, Deepali Mittal, Smeet Gala, Digant Gupta   +5 more
wiley   +1 more source

Pressure trasmission from the external ear canal to the inner ear - An experimental study on the incidental mechanism of perilymphatic fistulae.

, 1988
Shinsei Nishihara, Kiyofumi Gyo, Naoaki Yanagihara   +2 more
openalex   +2 more sources

Non-invasive Access to the Vagus Nerve Central Projections via Electrical Stimulation of the External Ear: fMRI Evidence in Humans

Brain Stimulation, 2015
E. Frangos, J. Ellrich, B. Komisaruk
semanticscholar   +1 more source

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää, Chad R. Haldeman‐Englert, Marja Hietala, Melisa S. Tanverdi, Patrick P. Koty, Diana Brightman, Eniolami Dosunmu, Shailja Tibrewal, Savleen Kaur, Anupriya Kaur, Raj Kumar Verma, Alejandra G. de Alba Campomanes, Virginia Utz, Anne M. Slavotinek, Cynthia Curry   +14 more
wiley   +1 more source

A Surprising Finding after External Ear Polypectomy in a Deaf Mute Patient [PDF]

, 2015
Hazem M. Abdel Tawab, Ravi Kumar, Salim M. Sloma Tabook   +2 more
openalex   +1 more source

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss, Amanda V. Karam, Julia Shalen, David E. Tunkel, Belina Y. Yi, Kelsey S. Guthrie, Emily M. Kudalkar, Anna E. Patrick, Sonja A. Rasmussen   +8 more
wiley   +1 more source

A Case Report of Ear Cholesteatoma with Osteoma in the External Auditory Canal.

, 1998
T. Sakamoto, Etsuo Yamamoto, Yasuyuki Tasaka, Tomoko Tsuji, Takayoshi Itaya, Syogo SHINOHARA, Norihiko Murai, Tesu Kim   +7 more
openalex   +2 more sources