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Anales Espanoles De Pediatria
|
March 23, 2001
[Gaucher's disease with D409H/D409H genotype. evolution with enzyme replacement therapy]
F Castelló Girona, C Domínguez Luengo, M del Toro Riera, et al.
Anales Espanoles De Pediatria
|
August 1, 1986
[Tubular handling of potassium in cystinosis]
F Castelló Girona, G Fortuny, L Callís Bracons, et al.
Anales Espanoles De Pediatria
|
June 5, 1999
[Results of treatment with oral citrate and pyridoxine in patients with primary hyperoxaluria type 1]
F Castelló Girona, E Riudor Taravilla, G Enríquez Civicos, et al.
Anales Espanoles De Pediatria
|
March 1, 1996
[Hyperprostaglandin E syndrome]
F Castelló Girona, D Yeste Fernández, E Vilaplana Cantó, et al.
Journal of Medical Genetics
|
September 11, 1998
Recurrence of the D409H mutation in Spanish Gaucher disease patients: description of a new homozygous patient and haplotype analysis
A Chabás, L Gort, M Montfort, et al.
The American Journal of Clinical Nutrition
|
January 5, 2000
Therapeutic effects of docosahexaenoic acid ethyl ester in patients with generalized peroxisomal disorders
M Martínez, E Vázquez, M T García-Silva, et al.
Revista De Neurologia
|
April 25, 2000
[Treatment of generalized peroxisomal disorders with docosahexaenoic acid ethyl ether]
M Martínez, E Vázquez, M T García-Silva, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Pearson syndrome: altered tricarboxylic acid and urea-cycle metabolites, adrenal insufficiency and corneal opacities
A Ribes, E Riudor, R Valcárel, et al.
Anales Espanoles De Pediatria
|
January 1, 1993
[Acute hemorrhagic edema in an infant]
D Yeste Fernández, U González Castro, J González Morla, et al.
Anales Espanoles De Pediatria
|
February 1, 1990
[Idiopathic infantile arterial calcification: diagnosis and treatment]
J A Balaguer Santamaría, J A García Conesa, C Goñi Oyaren, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
Anales Espanoles De Pediatria
|
March 23, 2001
[Gaucher's disease with D409H/D409H genotype. evolution with enzyme replacement therapy]
F Castelló Girona, C Domínguez Luengo, M del Toro Riera, et al.
Anales Espanoles De Pediatria
|
August 1, 1986
[Tubular handling of potassium in cystinosis]
F Castelló Girona, G Fortuny, L Callís Bracons, et al.
Anales Espanoles De Pediatria
|
June 5, 1999
[Results of treatment with oral citrate and pyridoxine in patients with primary hyperoxaluria type 1]
F Castelló Girona, E Riudor Taravilla, G Enríquez Civicos, et al.
Anales Espanoles De Pediatria
|
March 1, 1996
[Hyperprostaglandin E syndrome]
F Castelló Girona, D Yeste Fernández, E Vilaplana Cantó, et al.
Journal of Medical Genetics
|
September 11, 1998
Recurrence of the D409H mutation in Spanish Gaucher disease patients: description of a new homozygous patient and haplotype analysis
A Chabás, L Gort, M Montfort, et al.
The American Journal of Clinical Nutrition
|
January 5, 2000
Therapeutic effects of docosahexaenoic acid ethyl ester in patients with generalized peroxisomal disorders
M Martínez, E Vázquez, M T García-Silva, et al.
Revista De Neurologia
|
April 25, 2000
[Treatment of generalized peroxisomal disorders with docosahexaenoic acid ethyl ether]
M Martínez, E Vázquez, M T García-Silva, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Pearson syndrome: altered tricarboxylic acid and urea-cycle metabolites, adrenal insufficiency and corneal opacities
A Ribes, E Riudor, R Valcárel, et al.
Anales Espanoles De Pediatria
|
January 1, 1993
[Acute hemorrhagic edema in an infant]
D Yeste Fernández, U González Castro, J González Morla, et al.
Anales Espanoles De Pediatria
|
February 1, 1990
[Idiopathic infantile arterial calcification: diagnosis and treatment]
J A Balaguer Santamaría, J A García Conesa, C Goñi Oyaren, et al.
Page
of 3