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M Gennarelli

Showing results (21-30 of 71) with videos related to

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Molecular Psychiatry|March 13, 2001
Association between -G308A tumor necrosis factor alpha gene polymorphism and schizophreniaF Boin, R Zanardini, R Pioli, et al.
Prenatal Diagnosis|June 1, 1994
First-trimester prenatal diagnosis of spinal muscular atrophy using microsatellite markersS Lo Cicero, F Capon, S Melchionda, et al.
Pediatric Neurosurgery|September 1, 1996
Experimental acute subdural hematoma in infant pigletsE G Shaver, A C Duhaime, M Curtis, et al.
FEBS Letters|January 13, 1997
Expression of receptors for native and chemically modified low-density lipoproteins in brain microvesselsM Lucarelli, M Gennarelli, P Cardelli, et al.
Italian Journal of Neurological Sciences|February 1, 1996
Clinical and hormonal aspects of male hypogonadism in myotonic dystrophyI Mastrogiacomo, G Bonanni, E Menegazzo, et al.
Cell Biochemistry and Function|September 1, 1993
Isolation and cloning by a polymerase chain reaction of a genomic DNA fragment of the human slow skeletal troponin (TNNT1) geneG Novelli, M Gennarelli, F Sangiuolo, et al.
Molecular and Cellular Probes|June 1, 1993
A tool for the molecular analysis of an early lethal disease: slide-PCR in spinal muscular atrophy patientsF Capon, S Melchionda, M Gennarelli, et al.
Cell Biochemistry and Function|December 1, 1992
Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscleG Novelli, M Gennarelli, G Zelano, et al.
Biochemistry and Molecular Biology International|February 1, 1993
Failure in detecting mRNA transcripts from the mutated allele in myotonic dystrophy muscleG Novelli, M Gennarelli, G Zelano, et al.
Journal of Endocrinological Investigation|May 1, 1994
Male hypogonadism in myotonic dystrophy is related to (CTG)n triplet mutationI Mastrogiacomo, E Pagani, G Novelli, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
Molecular Psychiatry|March 13, 2001
Association between -G308A tumor necrosis factor alpha gene polymorphism and schizophreniaF Boin, R Zanardini, R Pioli, et al.
Prenatal Diagnosis|June 1, 1994
First-trimester prenatal diagnosis of spinal muscular atrophy using microsatellite markersS Lo Cicero, F Capon, S Melchionda, et al.
Pediatric Neurosurgery|September 1, 1996
Experimental acute subdural hematoma in infant pigletsE G Shaver, A C Duhaime, M Curtis, et al.
FEBS Letters|January 13, 1997
Expression of receptors for native and chemically modified low-density lipoproteins in brain microvesselsM Lucarelli, M Gennarelli, P Cardelli, et al.
Italian Journal of Neurological Sciences|February 1, 1996
Clinical and hormonal aspects of male hypogonadism in myotonic dystrophyI Mastrogiacomo, G Bonanni, E Menegazzo, et al.
Cell Biochemistry and Function|September 1, 1993
Isolation and cloning by a polymerase chain reaction of a genomic DNA fragment of the human slow skeletal troponin (TNNT1) geneG Novelli, M Gennarelli, F Sangiuolo, et al.
Molecular and Cellular Probes|June 1, 1993
A tool for the molecular analysis of an early lethal disease: slide-PCR in spinal muscular atrophy patientsF Capon, S Melchionda, M Gennarelli, et al.
Cell Biochemistry and Function|December 1, 1992
Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscleG Novelli, M Gennarelli, G Zelano, et al.
Biochemistry and Molecular Biology International|February 1, 1993
Failure in detecting mRNA transcripts from the mutated allele in myotonic dystrophy muscleG Novelli, M Gennarelli, G Zelano, et al.
Journal of Endocrinological Investigation|May 1, 1994
Male hypogonadism in myotonic dystrophy is related to (CTG)n triplet mutationI Mastrogiacomo, E Pagani, G Novelli, et al.
Pageof 8