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E Bertini

Showing results (1-10 of 205) with videos related to

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JAMA|May 28, 1982
Differential diagnosis of hypercalcemiaJ E Bertini
Journal of Molecular Medicine (Berlin, Germany)|October 1, 1996
Spinal muscular atrophies: recent insights and impact on molecular diagnosisC Brahe, E Bertini
Revista De Neurologia|April 2, 1999
[Congenital ataxias of genetic origin with structural anomalies of the cerebellum]E Bertini, J Campos-Castelló
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1995
Remission in dihydroxyphenylalanine-responsive dystoniaM Di Capua, E Bertini
Giornale Italiano Di Cardiologia|November 5, 1999
[Diagnosis of mitochondrial cardiomyopathies: the need for a multidisciplinary approach]F M Santorelli, E Bertini
Advances in Pediatrics|January 1, 1994
Hereditary metabolic cardiomyopathiesS Servidei, E Bertini, S DiMauro
Journal of Surgical Oncology|January 1, 1987
Renal cell carcinoma in a patient with situs inversus totalisJ E Bertini, M A Boileau
American Journal of Medical Genetics|October 23, 1995
Presymptomatic diagnosis of spinal muscular atrophy (SMA) III confirmed by deletion analysis of the survival motor neuron geneC Brahe, S Zappata, E Bertini
Brain & Development|September 1, 1992
Epilepsia partialis continua and neuronal migration anomaliesL Fusco, E Bertini, F Vigevano
Clinical Genetics|June 15, 2005
De novo alpha-actin mutations in monozygotic twinsC Graziano, E Bertini, B Porfirio
Pageof 21

Showing results (1-10 of 205) with videos related to

Sort By:
Pageof 21
JAMA|May 28, 1982
Differential diagnosis of hypercalcemiaJ E Bertini
Journal of Molecular Medicine (Berlin, Germany)|October 1, 1996
Spinal muscular atrophies: recent insights and impact on molecular diagnosisC Brahe, E Bertini
Revista De Neurologia|April 2, 1999
[Congenital ataxias of genetic origin with structural anomalies of the cerebellum]E Bertini, J Campos-Castelló
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1995
Remission in dihydroxyphenylalanine-responsive dystoniaM Di Capua, E Bertini
Giornale Italiano Di Cardiologia|November 5, 1999
[Diagnosis of mitochondrial cardiomyopathies: the need for a multidisciplinary approach]F M Santorelli, E Bertini
Advances in Pediatrics|January 1, 1994
Hereditary metabolic cardiomyopathiesS Servidei, E Bertini, S DiMauro
Journal of Surgical Oncology|January 1, 1987
Renal cell carcinoma in a patient with situs inversus totalisJ E Bertini, M A Boileau
American Journal of Medical Genetics|October 23, 1995
Presymptomatic diagnosis of spinal muscular atrophy (SMA) III confirmed by deletion analysis of the survival motor neuron geneC Brahe, S Zappata, E Bertini
Brain & Development|September 1, 1992
Epilepsia partialis continua and neuronal migration anomaliesL Fusco, E Bertini, F Vigevano
Clinical Genetics|June 15, 2005
De novo alpha-actin mutations in monozygotic twinsC Graziano, E Bertini, B Porfirio
Pageof 21