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American Journal of Medical Genetics. Part A
|
April 23, 2004
Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehog
Livia Garavelli, C Zanacca, G Caselli, et al.
Acta Bio-Medica : Atenei Parmensis
|
August 25, 2005
Albright's hereditary osteodystrophy (pseudohypoparathyroidism type Ia): clinical case with a novel mutation of GNAS1
Livia Garavelli, S Pedori, C Zanacca, 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.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
January 1, 1992
[Emergency endoscopy in children: experience of a digestive endoscopy department]
D Pacchione, M G Mortilla, E Ricci, et al.
L'Ateneo Parmense. Acta Bio-Medica : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
January 1, 1980
[Accidental poisoning in children. Epidemiological study and their prevention]
M Vanelli, G L de Angelis, N Caronna, et al.
Drugs
|
January 1, 1993
Double-blind study of nimesulide in divers with inflammatory disorders of the ear, nose and throat
G Banchini, I Scaricabarozzi, U Montecorboli, et al.
Panminerva Medica
|
October 1, 1980
Blood pressure levels related to age and puberal development at adolescence
R Virdis, S Bernasconi, M Rocca, et al.
Genetic Counseling (Geneva, Switzerland)
|
March 23, 2007
Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): report of a new Italian case with renal anomaly and review
L Garavelli, S Pedori, R Dal Zotto, 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.
Pediatric Dermatology
|
September 12, 2007
Dermatologic features in Pallister-Killian syndrome and their importance to the diagnosis
E Guareschi, L Garavelli, S Pedori, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 47) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics. Part A
|
April 23, 2004
Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehog
Livia Garavelli, C Zanacca, G Caselli, et al.
Acta Bio-Medica : Atenei Parmensis
|
August 25, 2005
Albright's hereditary osteodystrophy (pseudohypoparathyroidism type Ia): clinical case with a novel mutation of GNAS1
Livia Garavelli, S Pedori, C Zanacca, 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.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
January 1, 1992
[Emergency endoscopy in children: experience of a digestive endoscopy department]
D Pacchione, M G Mortilla, E Ricci, et al.
L'Ateneo Parmense. Acta Bio-Medica : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
January 1, 1980
[Accidental poisoning in children. Epidemiological study and their prevention]
M Vanelli, G L de Angelis, N Caronna, et al.
Drugs
|
January 1, 1993
Double-blind study of nimesulide in divers with inflammatory disorders of the ear, nose and throat
G Banchini, I Scaricabarozzi, U Montecorboli, et al.
Panminerva Medica
|
October 1, 1980
Blood pressure levels related to age and puberal development at adolescence
R Virdis, S Bernasconi, M Rocca, et al.
Genetic Counseling (Geneva, Switzerland)
|
March 23, 2007
Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): report of a new Italian case with renal anomaly and review
L Garavelli, S Pedori, R Dal Zotto, 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.
Pediatric Dermatology
|
September 12, 2007
Dermatologic features in Pallister-Killian syndrome and their importance to the diagnosis
E Guareschi, L Garavelli, S Pedori, et al.
Page
of 5