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Minerva Pediatrica
|
December 1, 1989
[Cohen syndrome. Description of a new case and study of the central nervous system using nuclear magnetic resonance]
O Gabrielli, C Pierleoni, M Barbato, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1993
[The importance of the clinical record in the follow-up of malformation syndromes]
O Gabrielli, G V Coppa, C Catassi, et al.
Minerva Pediatrica
|
August 31, 1978
[GM 1 gangliosidosis, type 1. Clinical description and biochemical study of a case]
G Coppa, A Maiorana, A Benincasa, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
November 24, 1999
Oligosaccharides in human milk during different phases of lactation
G V Coppa, P Pierani, L Zampini, et al.
International Journal of Molecular Medicine
|
September 24, 1999
Bone marrow transplantation in a Hunter patient with P266H mutation
G V Coppa, O Gabrielli, R Cordiali, et al.
Clinical Dysmorphology
|
May 29, 2000
Peculiar facies, obesity, cleft lip and palate, growth hormone deficiency and mental retardation: a new syndrome?
O Gabrielli, I Carloni, R Cordiali, et al.
American Journal of Medical Genetics
|
February 1, 1994
Stratton-Parker syndrome: confirmation of a new entity
O Gabrielli, I Carloni, C Catassi, et al.
Advances in Experimental Medicine and Biology
|
January 15, 2002
Characterization of oligosaccharides in milk and feces of breast-fed infants by high-performance anion-exchange chromatography
G V Coppa, P Pierani, L Zampini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1993
[Malformation syndromes and deafness]
V Bonifazi, O Gabrielli, L Ciferri, et al.
Pediatric Radiology
|
January 1, 1993
MRI appearances in amoebic granulomatous hepatitis: a case report
A Giovagnoni, O Gabrielli, G V Coppa, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 70) with videos related to
Sort By:
Page
of 7
Minerva Pediatrica
|
December 1, 1989
[Cohen syndrome. Description of a new case and study of the central nervous system using nuclear magnetic resonance]
O Gabrielli, C Pierleoni, M Barbato, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1993
[The importance of the clinical record in the follow-up of malformation syndromes]
O Gabrielli, G V Coppa, C Catassi, et al.
Minerva Pediatrica
|
August 31, 1978
[GM 1 gangliosidosis, type 1. Clinical description and biochemical study of a case]
G Coppa, A Maiorana, A Benincasa, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
November 24, 1999
Oligosaccharides in human milk during different phases of lactation
G V Coppa, P Pierani, L Zampini, et al.
International Journal of Molecular Medicine
|
September 24, 1999
Bone marrow transplantation in a Hunter patient with P266H mutation
G V Coppa, O Gabrielli, R Cordiali, et al.
Clinical Dysmorphology
|
May 29, 2000
Peculiar facies, obesity, cleft lip and palate, growth hormone deficiency and mental retardation: a new syndrome?
O Gabrielli, I Carloni, R Cordiali, et al.
American Journal of Medical Genetics
|
February 1, 1994
Stratton-Parker syndrome: confirmation of a new entity
O Gabrielli, I Carloni, C Catassi, et al.
Advances in Experimental Medicine and Biology
|
January 15, 2002
Characterization of oligosaccharides in milk and feces of breast-fed infants by high-performance anion-exchange chromatography
G V Coppa, P Pierani, L Zampini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1993
[Malformation syndromes and deafness]
V Bonifazi, O Gabrielli, L Ciferri, et al.
Pediatric Radiology
|
January 1, 1993
MRI appearances in amoebic granulomatous hepatitis: a case report
A Giovagnoni, O Gabrielli, G V Coppa, et al.
Page
of 7