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International Journal of Nanomedicine
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May 21, 2008
The mitochondrial genome, a growing interest inside an organelle
Marco Crimi, Roberta Rigolio
European Journal of Translational Myology
|
March 16, 2022
The genetic counseling in a patient affected by congenital polyneuropathy after a "diagnostic odyssey" recently solved with WES approach
Marco Crimi, Adnan Tarawneh
Frontiers in Public Health
|
November 24, 2022
Genome access and other web-based IT solutions: Genetic counseling in the digital era
Alessia Cazzaniga, Marta Plebani, Marco Crimi
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology
|
March 21, 2015
The challenge for a European network of biobanks for rare diseases taken up by RD-Connect
Lucia Monaco, Marco Crimi, Chiuhui Mary Wang
IUBMB Life
|
January 6, 2006
Molecular research technologies in mitochondrial diseases: the microarray approach
Marco Crimi, Sean F O'Hearn, Douglas C Wallace, et al.
Orphanet Journal of Rare Diseases
|
November 23, 2019
Experiences of patients with Poland syndrome of diagnosis and care in Italy: a pilot survey
Ilaria Baldelli, Fabio Gallo, Marco Crimi, et al.
Journal of Neuroscience Research
|
January 6, 2004
Retinoic acid-induced neuritogenesis of human neuroblastoma SH-SY5Y cells is ERK independent and PKC dependent
Mariarosaria Miloso, Daniela Villa, Marco Crimi, et al.
HGG Advances
|
October 3, 2022
The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes
Peining Li, Barbara Dupont, Qiping Hu, et al.
European Journal of Human Genetics : EJHG
|
October 23, 2003
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion
Marco Crimi, Roberto Del Bo, Sara Galbiati, et al.
Human Mutation
|
November 25, 2003
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions
Alessio Di Fonzo, Andreina Bordoni, Marco Crimi, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 32) with videos related to
Sort By:
Page
of 4
International Journal of Nanomedicine
|
May 21, 2008
The mitochondrial genome, a growing interest inside an organelle
Marco Crimi, Roberta Rigolio
European Journal of Translational Myology
|
March 16, 2022
The genetic counseling in a patient affected by congenital polyneuropathy after a "diagnostic odyssey" recently solved with WES approach
Marco Crimi, Adnan Tarawneh
Frontiers in Public Health
|
November 24, 2022
Genome access and other web-based IT solutions: Genetic counseling in the digital era
Alessia Cazzaniga, Marta Plebani, Marco Crimi
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology
|
March 21, 2015
The challenge for a European network of biobanks for rare diseases taken up by RD-Connect
Lucia Monaco, Marco Crimi, Chiuhui Mary Wang
IUBMB Life
|
January 6, 2006
Molecular research technologies in mitochondrial diseases: the microarray approach
Marco Crimi, Sean F O'Hearn, Douglas C Wallace, et al.
Orphanet Journal of Rare Diseases
|
November 23, 2019
Experiences of patients with Poland syndrome of diagnosis and care in Italy: a pilot survey
Ilaria Baldelli, Fabio Gallo, Marco Crimi, et al.
Journal of Neuroscience Research
|
January 6, 2004
Retinoic acid-induced neuritogenesis of human neuroblastoma SH-SY5Y cells is ERK independent and PKC dependent
Mariarosaria Miloso, Daniela Villa, Marco Crimi, et al.
HGG Advances
|
October 3, 2022
The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes
Peining Li, Barbara Dupont, Qiping Hu, et al.
European Journal of Human Genetics : EJHG
|
October 23, 2003
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion
Marco Crimi, Roberto Del Bo, Sara Galbiati, et al.
Human Mutation
|
November 25, 2003
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions
Alessio Di Fonzo, Andreina Bordoni, Marco Crimi, et al.
Page
of 4