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Reumatologia Clinica
|
July 29, 2011
[Effect of chondroitin sulfate and hyaluronic acid (500-730 kDa) on synthesis of stromelysin (MMP-3) and MMP-1 in human chondrocyte cultures]
J Monfort, M Nacher, E Montell, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 30, 2005
[Ghosal haematodiaphyseal dysplasia: a new case]
C Vignon-Savoye, M Le Merrer, A Vincens, et al.
Journal of Clinical Medicine
|
November 13, 2025
Cross-Cultural Validity and Reliability of the Questionnaire on Back-Health-Related Postural Habits During Daily Activities in the Polish Young Adolescent Population
Manuel Monfort-Pañego, Marta Kinga Labecka, Vicente Miñana-Signes, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine
|
June 4, 2013
[A KEL*02mod allele responsible for an apparent maternity exclusion]
M Monfort, T Peyrard, L Arnaud, et al.
Cadernos De Saude Publica
|
December 22, 2017
[Characterization of access to normal childbirth care in Bahia State, Brazil, based on graph theory]
Ludmilla Monfort Oliveira Sousa, Edna Maria de Araújo, José Garcia Vivas Miranda
Archives Francaises De Pediatrie
|
February 1, 1988
[Infantile polycystic disease. Renal pseudotumoral growth in the postnatal period]
M Monfort-Gouraud, P Sinnassamy, A Bensman, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
July 17, 2021
Simultaneous quantification of 19 analytes in breast milk by liquid chromatography-tandem mass spectrometry (LC-MS/MS)
Anaëlle Monfort, Martin Jutras, Brigitte Martin, et al.
Autoimmunity Reviews
|
February 20, 2021
Neuropsychiatric involvement in systemic lupus erythematosus: A review
Irene Carrión-Barberà, Tarek Carlos Salman-Monte, F Vílchez-Oya, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 13, 2014
Phenotype profiling of patients with intellectual disability and copy number variations
Mónica Roselló, Francisco Martínez, Sandra Monfort, et al.
American Journal of Medical Genetics. Part A
|
January 25, 2014
Duplication at Xq13.3-q21.1 with syndromic intellectual disability, a probable role for the ATRX gene
Francisco Martínez, Mónica Roselló, Sonia Mayo, et al.
Page
of 127
Search research articles
Search
Showing results (331-340 of 1,262) with videos related to
Sort By:
Page
of 127
Reumatologia Clinica
|
July 29, 2011
[Effect of chondroitin sulfate and hyaluronic acid (500-730 kDa) on synthesis of stromelysin (MMP-3) and MMP-1 in human chondrocyte cultures]
J Monfort, M Nacher, E Montell, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 30, 2005
[Ghosal haematodiaphyseal dysplasia: a new case]
C Vignon-Savoye, M Le Merrer, A Vincens, et al.
Journal of Clinical Medicine
|
November 13, 2025
Cross-Cultural Validity and Reliability of the Questionnaire on Back-Health-Related Postural Habits During Daily Activities in the Polish Young Adolescent Population
Manuel Monfort-Pañego, Marta Kinga Labecka, Vicente Miñana-Signes, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine
|
June 4, 2013
[A KEL*02mod allele responsible for an apparent maternity exclusion]
M Monfort, T Peyrard, L Arnaud, et al.
Cadernos De Saude Publica
|
December 22, 2017
[Characterization of access to normal childbirth care in Bahia State, Brazil, based on graph theory]
Ludmilla Monfort Oliveira Sousa, Edna Maria de Araújo, José Garcia Vivas Miranda
Archives Francaises De Pediatrie
|
February 1, 1988
[Infantile polycystic disease. Renal pseudotumoral growth in the postnatal period]
M Monfort-Gouraud, P Sinnassamy, A Bensman, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
July 17, 2021
Simultaneous quantification of 19 analytes in breast milk by liquid chromatography-tandem mass spectrometry (LC-MS/MS)
Anaëlle Monfort, Martin Jutras, Brigitte Martin, et al.
Autoimmunity Reviews
|
February 20, 2021
Neuropsychiatric involvement in systemic lupus erythematosus: A review
Irene Carrión-Barberà, Tarek Carlos Salman-Monte, F Vílchez-Oya, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 13, 2014
Phenotype profiling of patients with intellectual disability and copy number variations
Mónica Roselló, Francisco Martínez, Sandra Monfort, et al.
American Journal of Medical Genetics. Part A
|
January 25, 2014
Duplication at Xq13.3-q21.1 with syndromic intellectual disability, a probable role for the ATRX gene
Francisco Martínez, Mónica Roselló, Sonia Mayo, et al.
Page
of 127