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Annales De Dermatologie Et De Venereologie
|
January 1, 1989
[Leg ulcers and prolidase deficiency]
I Moulonguet, N Bamberger, G de Larrard, et al.
Presse Medicale (Paris, France : 1983)
|
June 16, 1984
[Acquired ichthyosis in the acquired immunodeficiency syndrome]
C Bories, C Blanchet-Bardon, J P Marie, et al.
Revue De Laryngologie - Otologie - Rhinologie
|
March 8, 2008
[Usher type I syndrome in children: genotype/phenotype correlation and cochlear implant benefits]
C Blanchet, A F Roux, C Hamel, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
January 1, 1991
Monoclonal antibody GB3 defines a widespread defect of several basement membranes and a keratinocyte dysfunction in patients with lethal junctional epidermolysis bullosa
P Verrando, C Blanchet-Bardon, A Pisani, et al.
Revue Des Maladies Respiratoires
|
April 11, 2000
[Respiratory manifestations after exposure to sulfurous anhydride in wine-cellar workers: 6 case reports]
F Testud, D Matray, R Lambert, et al.
Biochemistry
|
March 22, 2001
The "catalytic" triad of isocitrate dehydrogenase kinase/phosphatase from E. coli and its relationship with that found in eukaryotic protein kinases
C Oudot, J C Cortay, C Blanchet, et al.
Neuropsychiatrie De L'Enfance Et De L'Adolescence
|
February 22, 2021
[Adjustment of healthcare and telemedicine in times of lockdown and COVID-19 pandemic: Feedback from a "Maison des Adolescents" (Teenager's House)]
E Carretier, S B Guessoum, R Radjack, et al.
The Journal of Clinical Investigation
|
September 1, 1992
Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene
A Hovnanian, P Duquesnoy, C Blanchet-Bardon, et al.
The British Journal of Dermatology
|
March 24, 2000
Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French family
J Lamartine, D Laoudj, C Blanchet-Bardon, et al.
Medicine
|
January 1, 1993
Bullous amyloidosis. Report of 3 cases and review of the literature
C Robert, S Aractingi, C Prost, et al.
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of 20
Search research articles
Search
Showing results (161-170 of 200) with videos related to
Sort By:
Page
of 20
Annales De Dermatologie Et De Venereologie
|
January 1, 1989
[Leg ulcers and prolidase deficiency]
I Moulonguet, N Bamberger, G de Larrard, et al.
Presse Medicale (Paris, France : 1983)
|
June 16, 1984
[Acquired ichthyosis in the acquired immunodeficiency syndrome]
C Bories, C Blanchet-Bardon, J P Marie, et al.
Revue De Laryngologie - Otologie - Rhinologie
|
March 8, 2008
[Usher type I syndrome in children: genotype/phenotype correlation and cochlear implant benefits]
C Blanchet, A F Roux, C Hamel, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
January 1, 1991
Monoclonal antibody GB3 defines a widespread defect of several basement membranes and a keratinocyte dysfunction in patients with lethal junctional epidermolysis bullosa
P Verrando, C Blanchet-Bardon, A Pisani, et al.
Revue Des Maladies Respiratoires
|
April 11, 2000
[Respiratory manifestations after exposure to sulfurous anhydride in wine-cellar workers: 6 case reports]
F Testud, D Matray, R Lambert, et al.
Biochemistry
|
March 22, 2001
The "catalytic" triad of isocitrate dehydrogenase kinase/phosphatase from E. coli and its relationship with that found in eukaryotic protein kinases
C Oudot, J C Cortay, C Blanchet, et al.
Neuropsychiatrie De L'Enfance Et De L'Adolescence
|
February 22, 2021
[Adjustment of healthcare and telemedicine in times of lockdown and COVID-19 pandemic: Feedback from a "Maison des Adolescents" (Teenager's House)]
E Carretier, S B Guessoum, R Radjack, et al.
The Journal of Clinical Investigation
|
September 1, 1992
Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene
A Hovnanian, P Duquesnoy, C Blanchet-Bardon, et al.
The British Journal of Dermatology
|
March 24, 2000
Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French family
J Lamartine, D Laoudj, C Blanchet-Bardon, et al.
Medicine
|
January 1, 1993
Bullous amyloidosis. Report of 3 cases and review of the literature
C Robert, S Aractingi, C Prost, et al.
Page
of 20