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Neurology
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June 16, 2010
Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5p
C Depienne, E Magnin, D Bouteiller, et al.
La Nouvelle Presse Medicale
|
February 14, 1981
[Antenatal diagnosis of sickle-cell anaemia by DNA analysis of amniotic fluid cells. A preliminary study in the French West-Indies (author's transl)]
M Goossens, K Y Lee, A M Dozy, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
November 26, 2010
Familial young-onset forms of diabetes related to HNF4A and rare HNF1A molecular aetiologies
C Carette, D Dubois-Laforgue, C Saint-Martin, et al.
Brain : a Journal of Neurology
|
February 9, 2005
Cerebral venous sinus thrombosis in children: risk factors, presentation, diagnosis and outcome
G Sébire, B Tabarki, D E Saunders, et al.
Clinical Genetics
|
May 13, 2014
Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism
C Saint-Martin, Q Zhou, G M Martin, et al.
AJNR. American Journal of Neuroradiology
|
July 29, 2020
Characterizing the Subcortical Structures in Youth with Congenital Heart Disease
K Fontes, F Courtin, C V Rohlicek, et al.
Diabetes & Metabolism
|
March 11, 2015
High-sensitivity C-reactive protein does not improve the differential diagnosis of HNF1A-MODY and familial young-onset type 2 diabetes: A grey zone analysis
C Bellanné-Chantelot, J Coste, C Ciangura, et al.
Progress in Clinical and Biological Research
|
January 1, 1981
Isoelectric focusing of human hemoglobins
Y Beuzard, F Galacteros, F Braconnier, et al.
Breast Cancer Research and Treatment
|
September 6, 2019
Long-term survival in HER2-positive metastatic breast cancer treated with first-line trastuzumab: results from the french real-life curie database
E Kaczmarek, C Saint-Martin, J-Y Pierga, et al.
Journal of Medical Genetics
|
October 22, 2008
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
C Depienne, O Trouillard, C Saint-Martin, et al.
Page
of 5
Search research articles
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Showing results (31-40 of 47) with videos related to
Sort By:
Page
of 5
Neurology
|
June 16, 2010
Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5p
C Depienne, E Magnin, D Bouteiller, et al.
La Nouvelle Presse Medicale
|
February 14, 1981
[Antenatal diagnosis of sickle-cell anaemia by DNA analysis of amniotic fluid cells. A preliminary study in the French West-Indies (author's transl)]
M Goossens, K Y Lee, A M Dozy, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
November 26, 2010
Familial young-onset forms of diabetes related to HNF4A and rare HNF1A molecular aetiologies
C Carette, D Dubois-Laforgue, C Saint-Martin, et al.
Brain : a Journal of Neurology
|
February 9, 2005
Cerebral venous sinus thrombosis in children: risk factors, presentation, diagnosis and outcome
G Sébire, B Tabarki, D E Saunders, et al.
Clinical Genetics
|
May 13, 2014
Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism
C Saint-Martin, Q Zhou, G M Martin, et al.
AJNR. American Journal of Neuroradiology
|
July 29, 2020
Characterizing the Subcortical Structures in Youth with Congenital Heart Disease
K Fontes, F Courtin, C V Rohlicek, et al.
Diabetes & Metabolism
|
March 11, 2015
High-sensitivity C-reactive protein does not improve the differential diagnosis of HNF1A-MODY and familial young-onset type 2 diabetes: A grey zone analysis
C Bellanné-Chantelot, J Coste, C Ciangura, et al.
Progress in Clinical and Biological Research
|
January 1, 1981
Isoelectric focusing of human hemoglobins
Y Beuzard, F Galacteros, F Braconnier, et al.
Breast Cancer Research and Treatment
|
September 6, 2019
Long-term survival in HER2-positive metastatic breast cancer treated with first-line trastuzumab: results from the french real-life curie database
E Kaczmarek, C Saint-Martin, J-Y Pierga, et al.
Journal of Medical Genetics
|
October 22, 2008
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
C Depienne, O Trouillard, C Saint-Martin, et al.
Page
of 5