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Journal of Inherited Metabolic Disease
|
January 1, 1995
Immunological abnormalities in a patient with tyrosinaemia type III
P D D'Eufemia, R Finocchiaro, M Celli, et al.
Minerva Pediatrica
|
November 30, 1980
[Ocular diagnosis in hereditary lysosomal diseases]
A Cantani, A Ciarnella Cantani, O Giardini, et al.
Biology of the Neonate
|
January 1, 1979
Malonyldialdehyde formation, oxygen consumption, fatty acid composition in newborn platelets stimulated by thrombin
D Del Principe, M Gabriotti, F Mastracchio, et al.
Minerva Pediatrica
|
May 1, 1997
[Nailfold capillaroscopy in normal children between 0 and 16 years of age]
F Martino, D Agolini, D Aprigliano, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
January 1, 1981
[Glycogenosis type VI. Report of two cases (author's transl)]
P D'Eufemia, A Cantani, G Corrado, et al.
Acta Haematologica
|
January 1, 1978
Serum lipid pattern in beta-thalassaemia
O Giardini, F Murgia, F Martino, et al.
Journal of Pediatric Hematology/Oncology
|
October 19, 2000
Low-dosage immunoglobulins for an infant with hypogammaglobulinemia, maple syrup urine disease, and parvovirus B19-associated aplastic crisis
P D'Eufemia, G Nigro, M Celli, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications
|
November 26, 1999
Determination of urinary orotic acid and uracil by capillary zone electrophoresis
C Salerno, P D'Eufemia, M Celli, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1995
Low serum tryptophan to large neutral amino acids ratio in idiopathic infantile autism
P D'Eufemia, R Finocchiaro, M Celli, et al.
Minerva Pediatrica
|
April 30, 1980
[Hepatic histological and ultrastructural aspects of 2 cases of hereditary fructose intolerance]
A Ceccamea, F Nardi, T Faraggiana, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 93) with videos related to
Sort By:
Page
of 10
Journal of Inherited Metabolic Disease
|
January 1, 1995
Immunological abnormalities in a patient with tyrosinaemia type III
P D D'Eufemia, R Finocchiaro, M Celli, et al.
Minerva Pediatrica
|
November 30, 1980
[Ocular diagnosis in hereditary lysosomal diseases]
A Cantani, A Ciarnella Cantani, O Giardini, et al.
Biology of the Neonate
|
January 1, 1979
Malonyldialdehyde formation, oxygen consumption, fatty acid composition in newborn platelets stimulated by thrombin
D Del Principe, M Gabriotti, F Mastracchio, et al.
Minerva Pediatrica
|
May 1, 1997
[Nailfold capillaroscopy in normal children between 0 and 16 years of age]
F Martino, D Agolini, D Aprigliano, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
January 1, 1981
[Glycogenosis type VI. Report of two cases (author's transl)]
P D'Eufemia, A Cantani, G Corrado, et al.
Acta Haematologica
|
January 1, 1978
Serum lipid pattern in beta-thalassaemia
O Giardini, F Murgia, F Martino, et al.
Journal of Pediatric Hematology/Oncology
|
October 19, 2000
Low-dosage immunoglobulins for an infant with hypogammaglobulinemia, maple syrup urine disease, and parvovirus B19-associated aplastic crisis
P D'Eufemia, G Nigro, M Celli, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications
|
November 26, 1999
Determination of urinary orotic acid and uracil by capillary zone electrophoresis
C Salerno, P D'Eufemia, M Celli, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1995
Low serum tryptophan to large neutral amino acids ratio in idiopathic infantile autism
P D'Eufemia, R Finocchiaro, M Celli, et al.
Minerva Pediatrica
|
April 30, 1980
[Hepatic histological and ultrastructural aspects of 2 cases of hereditary fructose intolerance]
A Ceccamea, F Nardi, T Faraggiana, et al.
Page
of 10