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P Malaspina

Showing results (11-20 of 42) with videos related to

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Chemosphere|February 9, 2018
Combining spectroscopic techniques and chemometrics for the interpretation of lichen biomonitoring of air pollutionP Malaspina, M Casale, C Malegori, et al.
Annals of Human Genetics|October 1, 1990
The human Y chromosome shows a low level of DNA polymorphismP Malaspina, F Persichetti, A Novelletto, et al.
Neurochemistry International|June 18, 2016
Succinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolismP Malaspina, J-B Roullet, P L Pearl, et al.
American Journal of Human Genetics|July 31, 1998
Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)K L Chambliss, D D Hinson, F Trettel, et al.
Human Heredity|January 1, 1991
A further polymorphism of the Gd locus for glucose-6-phosphate dehydrogenase present among blacks (Nigerians) and apparently absent among Caucasoids: the quantitative isoelectrophoretic variation of the Gd+ alleleG Modiano, B M Ciminelli, P Malaspina, et al.
Human Genetics|July 1, 1990
Epidemiological and linkage studies on Huntington's disease in ItalyM Frontali, P Malaspina, C Rossi, et al.
Brain : a Journal of Neurology|August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxiasP Giunti, M G Sweeney, M Spadaro, et al.
Journal of Inherited Metabolic Disease|June 2, 2009
Visual evoked potentials in succinate semialdehyde dehydrogenase (SSADH) deficiencyG Di Rosa, P Malaspina, P Blasi, et al.
Genomics|September 15, 1996
Construction of a YAC contig covering human chromosome 6p22P Malaspina, A Roetto, F Trettel, et al.
American Journal of Physical Anthropology|November 2, 2006
Y-chromosomal variation in the Czech RepublicF Luca, F Di Giacomo, T Benincasa, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Chemosphere|February 9, 2018
Combining spectroscopic techniques and chemometrics for the interpretation of lichen biomonitoring of air pollutionP Malaspina, M Casale, C Malegori, et al.
Annals of Human Genetics|October 1, 1990
The human Y chromosome shows a low level of DNA polymorphismP Malaspina, F Persichetti, A Novelletto, et al.
Neurochemistry International|June 18, 2016
Succinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolismP Malaspina, J-B Roullet, P L Pearl, et al.
American Journal of Human Genetics|July 31, 1998
Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)K L Chambliss, D D Hinson, F Trettel, et al.
Human Heredity|January 1, 1991
A further polymorphism of the Gd locus for glucose-6-phosphate dehydrogenase present among blacks (Nigerians) and apparently absent among Caucasoids: the quantitative isoelectrophoretic variation of the Gd+ alleleG Modiano, B M Ciminelli, P Malaspina, et al.
Human Genetics|July 1, 1990
Epidemiological and linkage studies on Huntington's disease in ItalyM Frontali, P Malaspina, C Rossi, et al.
Brain : a Journal of Neurology|August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxiasP Giunti, M G Sweeney, M Spadaro, et al.
Journal of Inherited Metabolic Disease|June 2, 2009
Visual evoked potentials in succinate semialdehyde dehydrogenase (SSADH) deficiencyG Di Rosa, P Malaspina, P Blasi, et al.
Genomics|September 15, 1996
Construction of a YAC contig covering human chromosome 6p22P Malaspina, A Roetto, F Trettel, et al.
American Journal of Physical Anthropology|November 2, 2006
Y-chromosomal variation in the Czech RepublicF Luca, F Di Giacomo, T Benincasa, et al.
Pageof 5