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R Carrozzo

Showing results (1-10 of 76) with videos related to

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American Journal of Medical Genetics|October 2, 2001
Epilepsy and genetic malformations of the cerebral cortexR Guerrini, R Carrozzo
Seizure|December 26, 2001
Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testingR Guerrini, R Carrozzo
Journal of Bioenergetics and Biomembranes|April 1, 1997
Disorders of nuclear-mitochondrial intergenomic signallingM Zeviani, V Petruzzella, R Carrozzo
Brain & Development|April 17, 1998
Paroxysmal tonic upgaze of childhood with ataxia: a benign transient dystonia with autosomal dominant inheritanceR Guerrini, A Belmonte, R Carrozzo
Journal of Inherited Metabolic Disease|January 1, 1986
Protein-bound plasma homocyst(e)ine and identification of heterozygotes for cystathionine-synthase deficiencyR Sartorio, R Carrozzo, L Corbo, et al.
American Journal of Medical Genetics|September 5, 1997
High proportions of mtDNA duplications in patients with Kearns-Sayre syndrome occur in the heartB Fromenty, R Carrozzo, S Shanske, et al.
Clinical Genetics|April 1, 1988
A simplified test to detect PKU heterozygotes by discriminant analysis in mentally retarded children and their mothersR Sartorio, L Greco, R Carrozzo, et al.
FEBS Letters|December 20, 2000
The T9176G mutation of human mtDNA gives a fully assembled but inactive ATP synthase when modeled in Escherichia coliR Carrozzo, J Murray, F M Santorelli, et al.
JAMA|December 15, 1993
Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13W B Dobyns, O Reiner, R Carrozzo, et al.
American Journal of Medical Genetics|February 1, 1987
Megalocornea and mental retardation syndrome: two new casesE Del Giudice, R Sartorio, A Romano, et al.
Pageof 8

Showing results (1-10 of 76) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|October 2, 2001
Epilepsy and genetic malformations of the cerebral cortexR Guerrini, R Carrozzo
Seizure|December 26, 2001
Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testingR Guerrini, R Carrozzo
Journal of Bioenergetics and Biomembranes|April 1, 1997
Disorders of nuclear-mitochondrial intergenomic signallingM Zeviani, V Petruzzella, R Carrozzo
Brain & Development|April 17, 1998
Paroxysmal tonic upgaze of childhood with ataxia: a benign transient dystonia with autosomal dominant inheritanceR Guerrini, A Belmonte, R Carrozzo
Journal of Inherited Metabolic Disease|January 1, 1986
Protein-bound plasma homocyst(e)ine and identification of heterozygotes for cystathionine-synthase deficiencyR Sartorio, R Carrozzo, L Corbo, et al.
American Journal of Medical Genetics|September 5, 1997
High proportions of mtDNA duplications in patients with Kearns-Sayre syndrome occur in the heartB Fromenty, R Carrozzo, S Shanske, et al.
Clinical Genetics|April 1, 1988
A simplified test to detect PKU heterozygotes by discriminant analysis in mentally retarded children and their mothersR Sartorio, L Greco, R Carrozzo, et al.
FEBS Letters|December 20, 2000
The T9176G mutation of human mtDNA gives a fully assembled but inactive ATP synthase when modeled in Escherichia coliR Carrozzo, J Murray, F M Santorelli, et al.
JAMA|December 15, 1993
Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13W B Dobyns, O Reiner, R Carrozzo, et al.
American Journal of Medical Genetics|February 1, 1987
Megalocornea and mental retardation syndrome: two new casesE Del Giudice, R Sartorio, A Romano, et al.
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