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Rivista Dell'Infermiere
|
October 1, 1996
[Use of new forms for the evaluation of the clinical apprenticeship of nursing students]
S Rosini, A M Cotugno, G A De Gaetani, et al.
Toxics
|
August 12, 2018
Oxidative Stress in Methylmercury-Induced Cell Toxicity
Alessandra Antunes Dos Santos, Beatriz Ferrer, Filipe Marques Gonçalves, et al.
Neuroscience
|
January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architecture
I Meloni, V Parri, R De Filippis, et al.
Human Molecular Genetics
|
December 1, 1995
Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinism
M V Schiaffino, M T Bassi, L Galli, et al.
World Academy of Sciences Journal
|
April 30, 2020
Overview of the effects of chemical mixtures with endocrine disrupting activity in the context of real-life risk simulation: An integrative approach (Review)
Denisa Margina, George Mihai Nițulescu, Anca Ungurianu, et al.
Journal of Medical Genetics
|
January 15, 2003
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients
I Longo, S G M Frints, J-P Fryns, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
August 5, 2019
Long-term effects of chromium on morphological and immunological parameters of Wistar rats
A V Karaulov, E A Renieri, A I Smolyagin, et al.
European Neurology
|
February 28, 2004
Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular dystrophy
S Gambelli, A Malandrini, F Ginanneschi, et al.
Human Mutation
|
September 20, 2006
The Italian XLMR bank: a clinical and molecular database
C Pescucci, R Caselli, F Mari, et al.
Annals of Neurology
|
February 16, 1999
Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly
A Fogli, R Guerrini, F Moro, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 106) with videos related to
Sort By:
Page
of 11
Rivista Dell'Infermiere
|
October 1, 1996
[Use of new forms for the evaluation of the clinical apprenticeship of nursing students]
S Rosini, A M Cotugno, G A De Gaetani, et al.
Toxics
|
August 12, 2018
Oxidative Stress in Methylmercury-Induced Cell Toxicity
Alessandra Antunes Dos Santos, Beatriz Ferrer, Filipe Marques Gonçalves, et al.
Neuroscience
|
January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architecture
I Meloni, V Parri, R De Filippis, et al.
Human Molecular Genetics
|
December 1, 1995
Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinism
M V Schiaffino, M T Bassi, L Galli, et al.
World Academy of Sciences Journal
|
April 30, 2020
Overview of the effects of chemical mixtures with endocrine disrupting activity in the context of real-life risk simulation: An integrative approach (Review)
Denisa Margina, George Mihai Nițulescu, Anca Ungurianu, et al.
Journal of Medical Genetics
|
January 15, 2003
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients
I Longo, S G M Frints, J-P Fryns, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
August 5, 2019
Long-term effects of chromium on morphological and immunological parameters of Wistar rats
A V Karaulov, E A Renieri, A I Smolyagin, et al.
European Neurology
|
February 28, 2004
Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular dystrophy
S Gambelli, A Malandrini, F Ginanneschi, et al.
Human Mutation
|
September 20, 2006
The Italian XLMR bank: a clinical and molecular database
C Pescucci, R Caselli, F Mari, et al.
Annals of Neurology
|
February 16, 1999
Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly
A Fogli, R Guerrini, F Moro, et al.
Page
of 11