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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 14, 2003
[Acute immune epiduritis in a child]
R Boumpoutou, P Beze-Beyrie, B Guerin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 18, 2014
[Extrarespiratory manifestations of Mycoplasma pneumoniae: a case report]
E Guillet, C Mas, I Bauvin, et al.
The Journal of Urology
|
September 1, 1997
Bladder exstrophy: evaluation of factors leading to continence with spontaneous voiding after staged reconstruction
H B Lottmann, Y Melin, M Cendron, et al.
Neuropediatrics
|
February 12, 2021
Clinical Phenotype in an Early-Onset French Pediatric Population: Charcot-Marie-Tooth's Disease Type 2A
C Majorel-Beraud, E Baudou, U Walther-Louvier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 18, 2014
[Multicentric study of medical care and practices in spinal muscular atrophy type 1 over two 10-year periods]
C Barnérias, S Quijano, M Mayer, et al.
Journal of the Neurological Sciences
|
October 22, 2019
Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants
J Lerat, C Magdelaine, A Lunati, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 14, 2003
[Acute immune epiduritis in a child]
R Boumpoutou, P Beze-Beyrie, B Guerin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 18, 2014
[Extrarespiratory manifestations of Mycoplasma pneumoniae: a case report]
E Guillet, C Mas, I Bauvin, et al.
The Journal of Urology
|
September 1, 1997
Bladder exstrophy: evaluation of factors leading to continence with spontaneous voiding after staged reconstruction
H B Lottmann, Y Melin, M Cendron, et al.
Neuropediatrics
|
February 12, 2021
Clinical Phenotype in an Early-Onset French Pediatric Population: Charcot-Marie-Tooth's Disease Type 2A
C Majorel-Beraud, E Baudou, U Walther-Louvier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 18, 2014
[Multicentric study of medical care and practices in spinal muscular atrophy type 1 over two 10-year periods]
C Barnérias, S Quijano, M Mayer, et al.
Journal of the Neurological Sciences
|
October 22, 2019
Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants
J Lerat, C Magdelaine, A Lunati, et al.
Page
of 1