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Acta Clinica Belgica
|
August 19, 2015
Central skull base osteomyelitis: a rare but life-threatening disease
L Orioli, C Boute, P Eloy, et al.
Journal of Genetic Counseling
|
November 1, 2016
The Subjective Experience of Patients Diagnosed with Hereditary Hemorrhagic Telangiectasia: a Qualitative Study
Laura Geerts, Carole Fantini-Hauwel, Elodie Brugallé, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2004
Pre- and postnatal diagnosis of limb anomalies: a series of 107 cases
Muriel Holder-Espinasse, Louise Devisme, Dominique Thomas, et al.
Breast Cancer Research and Treatment
|
September 21, 2005
High grade primary breast lymphoma: is it a different clinical entity?
Christophe Fruchart, Yves Denoux, Jacques Chasle, et al.
Nature Genetics
|
March 31, 2000
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
N Boute, O Gribouval, S Roselli, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
|
February 24, 2001
Sudden rate drop intervention rate level in patients with new 'clarity' pacemakers and carotid sinus syndrome
S U Pavlovic, D Velimirovic, J van Hove, et al.
Geroscience
|
January 6, 2026
Heart failure with preserved ejection fraction shows no excess mortality in older patients: a population-matched relative survival analysis
Christophe de Terwangne, Nassiba Menghoum, Marin Boute, et al.
American Journal of Medical Genetics. Part A
|
July 22, 2014
Whole ARX gene duplication is compatible with normal intellectual development
Cornel Popovici, Tiffany Busa, Odile Boute, et al.
American Journal of Medical Genetics. Part A
|
August 7, 2013
Interstitial 12p13.1 deletion involving GRIN2B in three patients with intellectual disability
Sarra Dimassi, Joris Andrieux, Audrey Labalme, et al.
Clinical and Experimental Obstetrics & Gynecology
|
November 20, 2012
Assessment of fetomaternal hemorrhage by Kleihauer-Betke test, flow cytometry and α-fetoprotein after invasive obstetric procedures
D Meleti, A C R Caetano, T Boute, et al.
Page
of 24
Search research articles
Search
Showing results (111-120 of 232) with videos related to
Sort By:
Page
of 24
Acta Clinica Belgica
|
August 19, 2015
Central skull base osteomyelitis: a rare but life-threatening disease
L Orioli, C Boute, P Eloy, et al.
Journal of Genetic Counseling
|
November 1, 2016
The Subjective Experience of Patients Diagnosed with Hereditary Hemorrhagic Telangiectasia: a Qualitative Study
Laura Geerts, Carole Fantini-Hauwel, Elodie Brugallé, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2004
Pre- and postnatal diagnosis of limb anomalies: a series of 107 cases
Muriel Holder-Espinasse, Louise Devisme, Dominique Thomas, et al.
Breast Cancer Research and Treatment
|
September 21, 2005
High grade primary breast lymphoma: is it a different clinical entity?
Christophe Fruchart, Yves Denoux, Jacques Chasle, et al.
Nature Genetics
|
March 31, 2000
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
N Boute, O Gribouval, S Roselli, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
|
February 24, 2001
Sudden rate drop intervention rate level in patients with new 'clarity' pacemakers and carotid sinus syndrome
S U Pavlovic, D Velimirovic, J van Hove, et al.
Geroscience
|
January 6, 2026
Heart failure with preserved ejection fraction shows no excess mortality in older patients: a population-matched relative survival analysis
Christophe de Terwangne, Nassiba Menghoum, Marin Boute, et al.
American Journal of Medical Genetics. Part A
|
July 22, 2014
Whole ARX gene duplication is compatible with normal intellectual development
Cornel Popovici, Tiffany Busa, Odile Boute, et al.
American Journal of Medical Genetics. Part A
|
August 7, 2013
Interstitial 12p13.1 deletion involving GRIN2B in three patients with intellectual disability
Sarra Dimassi, Joris Andrieux, Audrey Labalme, et al.
Clinical and Experimental Obstetrics & Gynecology
|
November 20, 2012
Assessment of fetomaternal hemorrhage by Kleihauer-Betke test, flow cytometry and α-fetoprotein after invasive obstetric procedures
D Meleti, A C R Caetano, T Boute, et al.
Page
of 24