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Revue Neurologique
|
June 22, 2019
Charcot-Marie-Tooth (CMT)-like polyneuropathy revealing neurofibromatosis type 2: A case report and review of the literature
A Pegat, F Ducray, S Jeannin-Mayer, et al.
Annales De Dermatologie Et De Venereologie
|
November 6, 2007
[Utility of 18 FDG positon emission tomography in detection of sarcomatous transformation in neurofibromatosis type 1]
B Bensaid, F Giammarile, T Mognetti, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
June 20, 2000
[Cardiogenetics in the year 2000]
S Pinson, C Guichard, D Lenoir, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 30, 2009
[Usefulness of systematic brain magnetic resonance imaging in children with neurofibromatosis type 1]
G Blanchard, S Pinson, C Rousselle, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 3, 2014
[Type 2 neurofibromatosis: intergenerational differences in genetic and clinical expression]
A Drouet, F Le Moigne, D Salamé, et al.
Clinical Endocrinology
|
March 12, 2008
Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?
C Cardot-Bauters, E Leteurtre, L Leclerc, et al.
Annales De Dermatologie Et De Venereologie
|
June 8, 2001
[Neurofibromatosis 1: recommendations for management]
S Pinson, A Créange, S Barbarot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 28, 2002
[Neurofibromatosis 1: recommendations for management]
S Pinson, A Créange, S Barbarot, et al.
Journal Francais D'Ophtalmologie
|
May 16, 2002
[Recommendations for the treatment of neurofibromatosis type 1]
S Pinson, A Créange, S Barbarot, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Revue Neurologique
|
June 22, 2019
Charcot-Marie-Tooth (CMT)-like polyneuropathy revealing neurofibromatosis type 2: A case report and review of the literature
A Pegat, F Ducray, S Jeannin-Mayer, et al.
Annales De Dermatologie Et De Venereologie
|
November 6, 2007
[Utility of 18 FDG positon emission tomography in detection of sarcomatous transformation in neurofibromatosis type 1]
B Bensaid, F Giammarile, T Mognetti, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
June 20, 2000
[Cardiogenetics in the year 2000]
S Pinson, C Guichard, D Lenoir, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 30, 2009
[Usefulness of systematic brain magnetic resonance imaging in children with neurofibromatosis type 1]
G Blanchard, S Pinson, C Rousselle, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 3, 2014
[Type 2 neurofibromatosis: intergenerational differences in genetic and clinical expression]
A Drouet, F Le Moigne, D Salamé, et al.
Clinical Endocrinology
|
March 12, 2008
Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?
C Cardot-Bauters, E Leteurtre, L Leclerc, et al.
Annales De Dermatologie Et De Venereologie
|
June 8, 2001
[Neurofibromatosis 1: recommendations for management]
S Pinson, A Créange, S Barbarot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
February 28, 2002
[Neurofibromatosis 1: recommendations for management]
S Pinson, A Créange, S Barbarot, et al.
Journal Francais D'Ophtalmologie
|
May 16, 2002
[Recommendations for the treatment of neurofibromatosis type 1]
S Pinson, A Créange, S Barbarot, et al.
Page
of 2