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Virologie (Montrouge, France)
|
September 22, 2022
[Retrospective diagnosis of congenital cytomegalovirus infection in a deaf child using stored dried blood spots and real-time PCR assay]
M Leruez-Ville, N Loundon, A Ducroux, et al.
World Neurosurgery
|
August 14, 2017
IgG4-Related Disease: A New Etiology Underlying Diffuse Intracranial Dilating Vasculopathy
Evan S Marlin, David Dornbos, Daniel S Ikeda, et al.
Clinical Biochemistry
|
November 1, 2011
Molecular diagnosis of genetic deafness
L Jonard, S Marlin, M Louha, et al.
Advances in Experimental Medicine and Biology
|
January 8, 2021
Heimler Syndrome
S Mechaussier, I Perrault, H Dollfus, et al.
Lancet (London, England)
|
April 28, 1999
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling
F Denoyelle, S Marlin, D Weil, et al.
Journal of Neurosurgery. Pediatrics
|
May 3, 2014
Thoracolumbar spinal vascular malformation as a rare cause of isolated intraventricular hemorrhage
Evan S Marlin, John J Entwistle, Michael A Arnold, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
September 15, 2018
Myopia prevalence and risk factors in children
Christos Theophanous, Bobeck S Modjtahedi, Michael Batech, et al.
Inorganic Chemistry
|
October 14, 2003
Iron nitrosyls of a pentadentate ligand containing a single carboxamide group: syntheses, structures, electronic properties, and photolability of NO
Apurba K Patra, John M Rowland, Dana S Marlin, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
September 5, 2001
Connexin 26 gene mutations in congenitally deaf children: pitfalls for genetic counseling
S Marlin, E N Garabédian, G Roger, et al.
International Journal of Audiology
|
April 27, 2026
Transient disappearance of otoacoustic emissions after conventional hearing aid use in OTOF-related auditory neuropathy
S Bouzaïd, I Rouillon, P Avan, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 73) with videos related to
Sort By:
Page
of 8
Virologie (Montrouge, France)
|
September 22, 2022
[Retrospective diagnosis of congenital cytomegalovirus infection in a deaf child using stored dried blood spots and real-time PCR assay]
M Leruez-Ville, N Loundon, A Ducroux, et al.
World Neurosurgery
|
August 14, 2017
IgG4-Related Disease: A New Etiology Underlying Diffuse Intracranial Dilating Vasculopathy
Evan S Marlin, David Dornbos, Daniel S Ikeda, et al.
Clinical Biochemistry
|
November 1, 2011
Molecular diagnosis of genetic deafness
L Jonard, S Marlin, M Louha, et al.
Advances in Experimental Medicine and Biology
|
January 8, 2021
Heimler Syndrome
S Mechaussier, I Perrault, H Dollfus, et al.
Lancet (London, England)
|
April 28, 1999
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling
F Denoyelle, S Marlin, D Weil, et al.
Journal of Neurosurgery. Pediatrics
|
May 3, 2014
Thoracolumbar spinal vascular malformation as a rare cause of isolated intraventricular hemorrhage
Evan S Marlin, John J Entwistle, Michael A Arnold, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
September 15, 2018
Myopia prevalence and risk factors in children
Christos Theophanous, Bobeck S Modjtahedi, Michael Batech, et al.
Inorganic Chemistry
|
October 14, 2003
Iron nitrosyls of a pentadentate ligand containing a single carboxamide group: syntheses, structures, electronic properties, and photolability of NO
Apurba K Patra, John M Rowland, Dana S Marlin, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
September 5, 2001
Connexin 26 gene mutations in congenitally deaf children: pitfalls for genetic counseling
S Marlin, E N Garabédian, G Roger, et al.
International Journal of Audiology
|
April 27, 2026
Transient disappearance of otoacoustic emissions after conventional hearing aid use in OTOF-related auditory neuropathy
S Bouzaïd, I Rouillon, P Avan, et al.
Page
of 8