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Journal of Inherited Metabolic Disease
|
May 26, 2004
Clinical benefit in Fabry patients given enzyme replacement therapy--a case series
N Guffon, A Fouilhoux
La Revue De Medecine Interne
|
January 30, 2008
[Gaucher disease in childhood]
V Levrat, I Forest, A Fouilhoux, et al.
Journal Francais D'Ophtalmologie
|
March 16, 2005
[Relation between ocular manifestations and organ involvement in ten patients with Fabry disease]
L Fumex-Boizard, P Cochat, A Fouilhoux, et al.
Journal of the American Geriatrics Society
|
May 1, 1993
Dopamine B hydroxylase deficiency responsible for severe dysautonomic orthostatic hypotension in an elderly patient
A Gentric, A Fouilhoux, M Caroff, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 31, 2002
[Neurologic signs revealing a Behçet's disease: two pediatric case reports]
C Budin, B Ranchin, C Glastre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 29, 2001
[Eccrine neutrophilic hidradenitis: idiopathic plantar form in children]
T Erro-Vincent, A L Souillet, A Fouilhoux, et al.
Leukemia & Lymphoma
|
December 24, 1997
Bilateral eyelid localisation of a lymphoplasmacytoid lymphoma
M Fouassier, J M Menerath, F Tavernier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 7, 2005
[Netherton syndrome: a type of infantile erythroderma with failure to thrive, immune deficiency, rickets. Report of 3 cases]
E André, M Till, P Descargues, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 12, 2019
RMND1 mutations in two siblings: Severe renal hypoplasia but different levels of extrarenal abnormality severity: The ethics of decision making
E Broenen, B Ranchin, C Besmond, et al.
Orphanet Journal of Rare Diseases
|
February 1, 2021
Long term disease burden post-transplantation: three decades of observations in 25 Hurler patients successfully treated with hematopoietic stem cell transplantation (HSCT)
N Guffon, M Pettazzoni, N Pangaud, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
Journal of Inherited Metabolic Disease
|
May 26, 2004
Clinical benefit in Fabry patients given enzyme replacement therapy--a case series
N Guffon, A Fouilhoux
La Revue De Medecine Interne
|
January 30, 2008
[Gaucher disease in childhood]
V Levrat, I Forest, A Fouilhoux, et al.
Journal Francais D'Ophtalmologie
|
March 16, 2005
[Relation between ocular manifestations and organ involvement in ten patients with Fabry disease]
L Fumex-Boizard, P Cochat, A Fouilhoux, et al.
Journal of the American Geriatrics Society
|
May 1, 1993
Dopamine B hydroxylase deficiency responsible for severe dysautonomic orthostatic hypotension in an elderly patient
A Gentric, A Fouilhoux, M Caroff, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 31, 2002
[Neurologic signs revealing a Behçet's disease: two pediatric case reports]
C Budin, B Ranchin, C Glastre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 29, 2001
[Eccrine neutrophilic hidradenitis: idiopathic plantar form in children]
T Erro-Vincent, A L Souillet, A Fouilhoux, et al.
Leukemia & Lymphoma
|
December 24, 1997
Bilateral eyelid localisation of a lymphoplasmacytoid lymphoma
M Fouassier, J M Menerath, F Tavernier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 7, 2005
[Netherton syndrome: a type of infantile erythroderma with failure to thrive, immune deficiency, rickets. Report of 3 cases]
E André, M Till, P Descargues, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 12, 2019
RMND1 mutations in two siblings: Severe renal hypoplasia but different levels of extrarenal abnormality severity: The ethics of decision making
E Broenen, B Ranchin, C Besmond, et al.
Orphanet Journal of Rare Diseases
|
February 1, 2021
Long term disease burden post-transplantation: three decades of observations in 25 Hurler patients successfully treated with hematopoietic stem cell transplantation (HSCT)
N Guffon, M Pettazzoni, N Pangaud, et al.
Page
of 2