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The Hematology Journal : the Official Journal of the European Haematology Association
|
March 29, 2002
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis
G Tchernia, F Delhommeau, S Perrotta, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 4, 2004
[Disseminated lupus erythematosus in children: guidelines about investigations during the initial evaluation and follow-up]
B Bader-Meunier, E Haddad, P Niaudet, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
December 30, 2014
A large national cohort of French patients with chronic recurrent multifocal osteitis
J Wipff, F Costantino, I Lemelle, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 13, 2006
[Epidemiology of autoimmune haemolytic anemia in children: French data]
N Aladjidi, G Leverger, A Pariente, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
January 31, 2025
Assessment of Catheter-Directed Thrombolysis and Histotripsy Treatment for Deep Vein Thrombosis
Kevin Zhao, Erik Saucedo, Katia Flores Basterrechea, et al.
The Journal of Pediatrics
|
May 5, 2005
Initial presentation of childhood-onset systemic lupus erythematosus: a French multicenter study
B Bader-Meunier, J B Armengaud, E Haddad, et al.
Annals of the Rheumatic Diseases
|
August 24, 2011
Two-year results from an open-label, multicentre, phase III study evaluating the safety and efficacy of canakinumab in patients with cryopyrin-associated periodic syndrome across different severity phenotypes
Jasmin B Kuemmerle-Deschner, E Hachulla, R Cartwright, et al.
Journal of Medical Genetics
|
September 13, 2019
Distal hereditary motor neuronopathy of the Jerash type is caused by a novel <i>SIGMAR1</i> c.500A>T missense mutation
Antonis Ververis, Rana Dajani, Pantelitsa Koutsou, et al.
La Revue De Medecine Interne
|
September 21, 2023
French National Diagnostic and Care Protocol for antiphospholipid syndrome in adults and children
Z Amoura, B Bader-Meunier, C Bal Dit Sollier, et al.
Autoimmunity Reviews
|
January 7, 2022
A descriptive study of IgG4-related disease in children and young adults
B de Sainte Marie, M Ebbo, A Grados, et al.
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of 20
Search research articles
Search
Showing results (181-190 of 195) with videos related to
Sort By:
Page
of 20
The Hematology Journal : the Official Journal of the European Haematology Association
|
March 29, 2002
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis
G Tchernia, F Delhommeau, S Perrotta, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 4, 2004
[Disseminated lupus erythematosus in children: guidelines about investigations during the initial evaluation and follow-up]
B Bader-Meunier, E Haddad, P Niaudet, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
December 30, 2014
A large national cohort of French patients with chronic recurrent multifocal osteitis
J Wipff, F Costantino, I Lemelle, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 13, 2006
[Epidemiology of autoimmune haemolytic anemia in children: French data]
N Aladjidi, G Leverger, A Pariente, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
January 31, 2025
Assessment of Catheter-Directed Thrombolysis and Histotripsy Treatment for Deep Vein Thrombosis
Kevin Zhao, Erik Saucedo, Katia Flores Basterrechea, et al.
The Journal of Pediatrics
|
May 5, 2005
Initial presentation of childhood-onset systemic lupus erythematosus: a French multicenter study
B Bader-Meunier, J B Armengaud, E Haddad, et al.
Annals of the Rheumatic Diseases
|
August 24, 2011
Two-year results from an open-label, multicentre, phase III study evaluating the safety and efficacy of canakinumab in patients with cryopyrin-associated periodic syndrome across different severity phenotypes
Jasmin B Kuemmerle-Deschner, E Hachulla, R Cartwright, et al.
Journal of Medical Genetics
|
September 13, 2019
Distal hereditary motor neuronopathy of the Jerash type is caused by a novel <i>SIGMAR1</i> c.500A>T missense mutation
Antonis Ververis, Rana Dajani, Pantelitsa Koutsou, et al.
La Revue De Medecine Interne
|
September 21, 2023
French National Diagnostic and Care Protocol for antiphospholipid syndrome in adults and children
Z Amoura, B Bader-Meunier, C Bal Dit Sollier, et al.
Autoimmunity Reviews
|
January 7, 2022
A descriptive study of IgG4-related disease in children and young adults
B de Sainte Marie, M Ebbo, A Grados, et al.
Page
of 20