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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
July 1, 1985
[Gastro-esophageal reflux in childhood. When to operate?]
C Del Rossi, S Scuto, M Mori, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1985
[Varicocele in childhood]
G Cerasoli, U Beseghi, C Del Rossi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
October 12, 2001
[Surgery of congenital malformations in developing countries: experience in 13 humanitarian missions during 9 years]
S d'Agostino, C Del Rossi, S Del Curto, et al.
Minerva Dietologica E Gastroenterologica
|
April 1, 1979
[Indications and results of parenteral nutrition in the surgical treatment of neoplastic stenosis of the esophagus and cardia]
P Bobbio, E Foggi, C Del Rossi, et al.
Journal of Endocrinological Investigation
|
April 1, 1981
Effects of somatostatin in a case of severe hypoglycemia due to nesidioblastosis
E Roti, C Ghinelli, P Bandini, et al.
Archives Francaises De Pediatrie
|
November 1, 1987
[Intraluminal diverticulum of the duodenum]
C Ghinelli, M Vitali, C Del Rossi, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
January 1, 1985
[Indications for diagnostic and surgical digestive endoscopy in childhood: personal clinical experience]
S Scuto, C Del Rossi, U Beseghi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
September 1, 1983
[Clinical approach to constipation: proposal of a diagnostic and therapeutic protocol]
G L de Angelis, C Ghinelli, G Gregori, et al.
Anales Espanoles De Pediatria
|
November 1, 1983
[Gastric acidity and serum levels of pepsinogen I and gastrin in children with primary duodenal ulcer]
C Ghinelli, S Scuto, G Banchini, et al.
American Journal of Medical Genetics. Part A
|
January 11, 2003
Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome
L Garavelli, A Donadio, C Zanacca, et al.
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of 3
Search research articles
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Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
July 1, 1985
[Gastro-esophageal reflux in childhood. When to operate?]
C Del Rossi, S Scuto, M Mori, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1985
[Varicocele in childhood]
G Cerasoli, U Beseghi, C Del Rossi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
October 12, 2001
[Surgery of congenital malformations in developing countries: experience in 13 humanitarian missions during 9 years]
S d'Agostino, C Del Rossi, S Del Curto, et al.
Minerva Dietologica E Gastroenterologica
|
April 1, 1979
[Indications and results of parenteral nutrition in the surgical treatment of neoplastic stenosis of the esophagus and cardia]
P Bobbio, E Foggi, C Del Rossi, et al.
Journal of Endocrinological Investigation
|
April 1, 1981
Effects of somatostatin in a case of severe hypoglycemia due to nesidioblastosis
E Roti, C Ghinelli, P Bandini, et al.
Archives Francaises De Pediatrie
|
November 1, 1987
[Intraluminal diverticulum of the duodenum]
C Ghinelli, M Vitali, C Del Rossi, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
January 1, 1985
[Indications for diagnostic and surgical digestive endoscopy in childhood: personal clinical experience]
S Scuto, C Del Rossi, U Beseghi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
September 1, 1983
[Clinical approach to constipation: proposal of a diagnostic and therapeutic protocol]
G L de Angelis, C Ghinelli, G Gregori, et al.
Anales Espanoles De Pediatria
|
November 1, 1983
[Gastric acidity and serum levels of pepsinogen I and gastrin in children with primary duodenal ulcer]
C Ghinelli, S Scuto, G Banchini, et al.
American Journal of Medical Genetics. Part A
|
January 11, 2003
Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome
L Garavelli, A Donadio, C Zanacca, et al.
Page
of 3