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Showing results (41-50 of 47) with videos related to

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Neuropediatrics|May 7, 2010
Massive hemobilia and papillomatosis of the gallbladder in metachromatic leukodystrophy: a life-threatening conditionL Garavelli, S Rosato, A Mele, et al.
Hormone Research|May 24, 2005
Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and reviewL Garavelli, P Cerruti-Mainardi, R Virdis, et al.
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literatureL Garavelli, K Leask, C Zanacca, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Mandibuloacral dysplasia type A in childhoodL Garavelli, M R D'Apice, F Rivieri, et al.
Neuropediatrics|December 7, 2007
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new caseL Garavelli, E Guareschi, S Errico, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 1, 1997
A multicentre study on behalf of the European Society of Paediatric Gastroenterology and Nutrition Working Group on Acute Diarrhoea. Early feeding in childhood gastroenteritisB K Sandhu, E Isolauri, J A Walker-Smith, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 1, 1997
Guidelines prepared by the ESPGAN Working Group on Acute Diarrhoea. Recommendations for feeding in childhood gastroenteritis. European Society of Pediatric Gastroenterology and NutritionJ A Walker-Smith, B K Sandhu, E Isolauri, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Neuropediatrics|May 7, 2010
Massive hemobilia and papillomatosis of the gallbladder in metachromatic leukodystrophy: a life-threatening conditionL Garavelli, S Rosato, A Mele, et al.
Hormone Research|May 24, 2005
Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and reviewL Garavelli, P Cerruti-Mainardi, R Virdis, et al.
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literatureL Garavelli, K Leask, C Zanacca, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Mandibuloacral dysplasia type A in childhoodL Garavelli, M R D'Apice, F Rivieri, et al.
Neuropediatrics|December 7, 2007
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new caseL Garavelli, E Guareschi, S Errico, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 1, 1997
A multicentre study on behalf of the European Society of Paediatric Gastroenterology and Nutrition Working Group on Acute Diarrhoea. Early feeding in childhood gastroenteritisB K Sandhu, E Isolauri, J A Walker-Smith, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 1, 1997
Guidelines prepared by the ESPGAN Working Group on Acute Diarrhoea. Recommendations for feeding in childhood gastroenteritis. European Society of Pediatric Gastroenterology and NutritionJ A Walker-Smith, B K Sandhu, E Isolauri, et al.
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