Showing results (21-30 of 103) with videos related to
Sort By:
Pageof 11
Medical & Biological Engineering & Computing|May 1, 1997
Continuous measurements by impedance of haematocrit and plasma volume variations during dialysisM Maasrani, M Y Jaffrin, B BoudailliezThe International Journal of Artificial Organs|March 1, 1995
Urea, creatinine and phosphate kinetic modeling during dialysis: application to pediatric hemodialysisM Maasrani, M Y Jaffrin, M Fischbach, et al.Neuropsychiatrie De L'Enfance Et De L'Adolescence|June 9, 2023
[Covid-19 and adolescence: Clinical findings and psychopathological thoughts about some immediate or differed impacts]C Mille, B Boudailliez, S Garny de La RivièreAnnales De Genetique|January 1, 1980
[Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)]E Obry, C Piussan, B Risbourg, et al.Archives Francaises De Pediatrie|November 1, 1990
[Waardenburg's syndrome and severe cyanotic cardiopathy]M Mathieu, E Bourges, F Caron, et al.Archives Francaises De Pediatrie|June 1, 1975
[Bone dysplasia with dwarfism and diffuse skeletal alterations]C Piussan, P Maroteaux, I Castroviejo, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 28, 2003
[Change in management of ureteropelvic junction obstruction]P Buisson, J Ricard, B Boudailliez, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardationM Mathieu, A De Broca, H Bony, et al.American Journal of Medical Genetics|August 9, 1996
Fragile X mutation and FG syndrome-like phenotypeC Piussan, M Mathieu, P Berquin, et al.Medical & Biological Engineering & Computing|May 1, 1997
Extra- and intracellular volume monitoring by impedance during haemodialysis using Cole-Cole extrapolationM Y Jaffrin, M Maasrani, A Le Gourrier, et al.Pageof 11