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L Garavelli

Showing results (101-110 of 116) with videos related to

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Emerging Infectious Diseases|May 3, 2011
Imported dengue virus serotype 3, Yemen to Italy, 2010Paolo Ravanini, Eili Huhtamo, Essi Hasu, et al.
European Journal of Epidemiology|September 17, 2003
Congenital heart defects: 15 years of experience of the Emilia-Romagna Registry (Italy)E Calzolari, G Garani, G Cocchi, 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 reviewL 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 syndromeL Garavelli, A Donadio, C Zanacca, et al.
Pediatric Dermatology|September 12, 2007
Dermatologic features in Pallister-Killian syndrome and their importance to the diagnosisE Guareschi, L Garavelli, S Pedori, et al.
Neuropediatrics|April 12, 2018
A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and HydrocephalusI Maini, E Farnetti, S G Caraffi, et al.
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.
American Journal of Medical Genetics. Part A|March 21, 2008
Holt-Oram syndrome associated with anomalies of the feetL Garavelli, D De Brasi, R Verri, 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.
Pageof 12

Showing results (101-110 of 116) with videos related to

Sort By:
Pageof 12
Emerging Infectious Diseases|May 3, 2011
Imported dengue virus serotype 3, Yemen to Italy, 2010Paolo Ravanini, Eili Huhtamo, Essi Hasu, et al.
European Journal of Epidemiology|September 17, 2003
Congenital heart defects: 15 years of experience of the Emilia-Romagna Registry (Italy)E Calzolari, G Garani, G Cocchi, 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 reviewL 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 syndromeL Garavelli, A Donadio, C Zanacca, et al.
Pediatric Dermatology|September 12, 2007
Dermatologic features in Pallister-Killian syndrome and their importance to the diagnosisE Guareschi, L Garavelli, S Pedori, et al.
Neuropediatrics|April 12, 2018
A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and HydrocephalusI Maini, E Farnetti, S G Caraffi, et al.
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.
American Journal of Medical Genetics. Part A|March 21, 2008
Holt-Oram syndrome associated with anomalies of the feetL Garavelli, D De Brasi, R Verri, 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.
Pageof 12