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P S Jouk

Showing results (41-50 of 61) with videos related to

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Pediatrie|March 1, 1985
[Diagnosis and treatment of fetal tachycardia. Apropos of 2 cases]P S Jouk, A M Rossignol, D André, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|November 20, 2004
[Kell alloimmunization in pregnancy]S Gariod, Y Brossard, M-H Poissonnier, et al.
Pediatrie|April 1, 1986
[Digitalis poisoning in children. Treatment with anti-digoxin Fab antibody fragments. Apropos of a case and a discussion of therapeutic indications]P S Jouk, V Danel, M Bovier-Lapierre, et al.
Fetal Diagnosis and Therapy|June 5, 2010
Brachytelephalangic chondrodysplasia punctata: prenatal diagnosis and postnatal outcomeS Boulet, K Dieterich, M Althuser, et al.
Journal of Medical Genetics|May 19, 2001
A heterozygous endothelin 3 mutation in Waardenburg-Hirschsprung disease: is there a dosage effect of EDN3/EDNRB gene mutations on neurocristopathy phenotypes?V Pingault, N Bondurand, N Lemort, et al.
Journal of Intellectual Disability Research : JIDR|June 12, 2013
Prevalence and characteristics of children with mild intellectual disability in a French countyM David, K Dieterich, A Billette de Villemeur, et al.
Clinical Genetics|March 26, 2013
190-kb duplication in 1p36.11 including PIGV and ARID1A genes in a girl with intellectual disability and hexadactylyC Coutton, M Bidart, J Rendu, et al.
Seizure|May 25, 2002
So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutationV des Portes, L Abaoub, A Joannard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 28, 2002
[Congenital toxoplasmosis: prevention in the pregnant woman and management of the neonate]H Pelloux, H Fricker-Hidalgo, J C Pons, et al.
Molecular Syndromology|February 20, 2014
Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH GeneC Coutton, B Poreau, F Devillard, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Pediatrie|March 1, 1985
[Diagnosis and treatment of fetal tachycardia. Apropos of 2 cases]P S Jouk, A M Rossignol, D André, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|November 20, 2004
[Kell alloimmunization in pregnancy]S Gariod, Y Brossard, M-H Poissonnier, et al.
Pediatrie|April 1, 1986
[Digitalis poisoning in children. Treatment with anti-digoxin Fab antibody fragments. Apropos of a case and a discussion of therapeutic indications]P S Jouk, V Danel, M Bovier-Lapierre, et al.
Fetal Diagnosis and Therapy|June 5, 2010
Brachytelephalangic chondrodysplasia punctata: prenatal diagnosis and postnatal outcomeS Boulet, K Dieterich, M Althuser, et al.
Journal of Medical Genetics|May 19, 2001
A heterozygous endothelin 3 mutation in Waardenburg-Hirschsprung disease: is there a dosage effect of EDN3/EDNRB gene mutations on neurocristopathy phenotypes?V Pingault, N Bondurand, N Lemort, et al.
Journal of Intellectual Disability Research : JIDR|June 12, 2013
Prevalence and characteristics of children with mild intellectual disability in a French countyM David, K Dieterich, A Billette de Villemeur, et al.
Clinical Genetics|March 26, 2013
190-kb duplication in 1p36.11 including PIGV and ARID1A genes in a girl with intellectual disability and hexadactylyC Coutton, M Bidart, J Rendu, et al.
Seizure|May 25, 2002
So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutationV des Portes, L Abaoub, A Joannard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 28, 2002
[Congenital toxoplasmosis: prevention in the pregnant woman and management of the neonate]H Pelloux, H Fricker-Hidalgo, J C Pons, et al.
Molecular Syndromology|February 20, 2014
Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH GeneC Coutton, B Poreau, F Devillard, et al.
Pageof 7