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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 1, 1996
[Mitochondrial cytopathies: identification of responsible nuclear genes]
V Paquis
Neurology
|
July 1, 1997
Cerebral infarction associated with Kearns-Sayre syndrome
B Chabrol, V Paquis
Revue Neurologique
|
May 6, 2014
An overview of neurological and neuromuscular signs in mitochondrial diseases
A Chaussenot, V Paquis-Flucklinger
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 28, 2020
Molecular diagnosis and genetic counseling for spinal muscular atrophy (SMA)
C Rouzier, A Chaussenot, V Paquis-Flucklinger
Diabetes & Metabolism
|
March 1, 1997
Clinical aspects of mitochondrial diabetes
B Vialettes, V Paquis-Flucklinger, D Bendahan
The American Journal of Pathology
|
March 1, 1994
Experimental Sertoli cell tumors in the mouse and their progression into a mixed germ cell-sex cord proliferation
V Paquis-Flucklinger, M Rassoulzadegan, J F Michiels
Gynecologie, Obstetrique & Fertilite
|
June 5, 2007
[Newborn of HIV positive grandmother: reasons to be delighted or reasons to worry?]
J Delotte, F Monpoux, V Paquis-Flucklinger, et al.
Annales D'Endocrinologie
|
July 1, 2005
[Monogenic diabetes: a useful dimension for diabetology practice]
R Valéro, S Béliard, V Paquis-Fluckinger, et al.
Journal De Genetique Humaine
|
June 1, 1989
[Expressivity of familial forms of Fraser syndrome]
J C Lambert, I Touitou, V Paquis, et al.
Revue Neurologique
|
June 21, 2008
[Diagnostic and prognostic values of 1p and 19q deletions in adult gliomas: critical review of the literature and implications in daily clinical practice]
D Fontaine, F Vandenbos, C Lebrun, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 61) with videos related to
Sort By:
Page
of 7
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 1, 1996
[Mitochondrial cytopathies: identification of responsible nuclear genes]
V Paquis
Neurology
|
July 1, 1997
Cerebral infarction associated with Kearns-Sayre syndrome
B Chabrol, V Paquis
Revue Neurologique
|
May 6, 2014
An overview of neurological and neuromuscular signs in mitochondrial diseases
A Chaussenot, V Paquis-Flucklinger
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 28, 2020
Molecular diagnosis and genetic counseling for spinal muscular atrophy (SMA)
C Rouzier, A Chaussenot, V Paquis-Flucklinger
Diabetes & Metabolism
|
March 1, 1997
Clinical aspects of mitochondrial diabetes
B Vialettes, V Paquis-Flucklinger, D Bendahan
The American Journal of Pathology
|
March 1, 1994
Experimental Sertoli cell tumors in the mouse and their progression into a mixed germ cell-sex cord proliferation
V Paquis-Flucklinger, M Rassoulzadegan, J F Michiels
Gynecologie, Obstetrique & Fertilite
|
June 5, 2007
[Newborn of HIV positive grandmother: reasons to be delighted or reasons to worry?]
J Delotte, F Monpoux, V Paquis-Flucklinger, et al.
Annales D'Endocrinologie
|
July 1, 2005
[Monogenic diabetes: a useful dimension for diabetology practice]
R Valéro, S Béliard, V Paquis-Fluckinger, et al.
Journal De Genetique Humaine
|
June 1, 1989
[Expressivity of familial forms of Fraser syndrome]
J C Lambert, I Touitou, V Paquis, et al.
Revue Neurologique
|
June 21, 2008
[Diagnostic and prognostic values of 1p and 19q deletions in adult gliomas: critical review of the literature and implications in daily clinical practice]
D Fontaine, F Vandenbos, C Lebrun, et al.
Page
of 7