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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 5, 2001
[Dysmorphic syndromes at birth: what to do?]
C Baumann, D Héron
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 22, 2023
Management of atopic dermatitis by pediatricians: A French national survey-based study
D Héron, A Nosbaum, C Braun
Revue Neurologique
|
April 6, 2013
[Family impact of FXTAS diagnosis: genetic counseling for at-risk relatives]
G Lesca, S Lejeune, D Hernette, et al.
Journal of Medical Genetics
|
August 1, 1995
Filippi syndrome: a new case with skeletal abnormalities
D Héron, T Billette de Villemeur, A Munnich, et al.
American Journal of Medical Genetics
|
November 6, 1995
Sternal cleft: case report and review of a series of nine patients
D Héron, S Lyonnet, L Iserin, et al.
L'Encephale
|
April 11, 2001
[Microdeletion 22q11: apropos of case of schizophrenia in an adolescent]
C Pinquier, D Héron, W de Carvalho, et al.
Pediatric Neurosurgery
|
July 1, 1996
A male fetus with aqueductal stenosis and four accessory spleens. A case report with a tentative genetic explanation
M Catala, V Aubert, S Lesourd, et al.
La Revue De Medecine Interne
|
December 12, 2018
[Retrospective analysis of anti-TIF1gamma, anti-NXP2 and anti-SAE1/2 antibodies carriers at Bordeaux university hospital from November 2014 to February 2017]
J Victor, L Zanardo, D Héron-Mermin, et al.
Neuromuscular Disorders : NMD
|
January 24, 2018
Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity?
N Angeard, E Huerta, A Jacquette, et al.
Blood
|
July 27, 2000
Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)
C Valentin, S Pissard, J Martin, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 5, 2001
[Dysmorphic syndromes at birth: what to do?]
C Baumann, D Héron
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 22, 2023
Management of atopic dermatitis by pediatricians: A French national survey-based study
D Héron, A Nosbaum, C Braun
Revue Neurologique
|
April 6, 2013
[Family impact of FXTAS diagnosis: genetic counseling for at-risk relatives]
G Lesca, S Lejeune, D Hernette, et al.
Journal of Medical Genetics
|
August 1, 1995
Filippi syndrome: a new case with skeletal abnormalities
D Héron, T Billette de Villemeur, A Munnich, et al.
American Journal of Medical Genetics
|
November 6, 1995
Sternal cleft: case report and review of a series of nine patients
D Héron, S Lyonnet, L Iserin, et al.
L'Encephale
|
April 11, 2001
[Microdeletion 22q11: apropos of case of schizophrenia in an adolescent]
C Pinquier, D Héron, W de Carvalho, et al.
Pediatric Neurosurgery
|
July 1, 1996
A male fetus with aqueductal stenosis and four accessory spleens. A case report with a tentative genetic explanation
M Catala, V Aubert, S Lesourd, et al.
La Revue De Medecine Interne
|
December 12, 2018
[Retrospective analysis of anti-TIF1gamma, anti-NXP2 and anti-SAE1/2 antibodies carriers at Bordeaux university hospital from November 2014 to February 2017]
J Victor, L Zanardo, D Héron-Mermin, et al.
Neuromuscular Disorders : NMD
|
January 24, 2018
Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity?
N Angeard, E Huerta, A Jacquette, et al.
Blood
|
July 27, 2000
Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)
C Valentin, S Pissard, J Martin, et al.
Page
of 3