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The Journal of Nutrition, Health & Aging
|
April 14, 2012
Screening for frailty in elderly emergency department patients by using the Identification of Seniors At Risk (ISAR)
F Salvi, V Morichi, A Grilli, et al.
Annals of Neurology
|
August 1, 1995
An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
M Ragno, E Tournier-Lasserve, M G Fiori, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 20, 2007
Brain structural damage in Friedreich's ataxia
R Della Nave, A Ginestroni, M Giannelli, et al.
Clinical Genetics
|
June 14, 2000
Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel hot spot' in codon 47
A Ferlini, L Obici, E Manzati, et al.
International Journal of Radiation Oncology, Biology, Physics
|
February 8, 2000
Radiation-induced gadd45 expression correlates with clinical response to radiotherapy of cervical carcinoma
M A Santucci, E Barbieri, G Frezza, et al.
Il Giornale Di Chirurgia
|
March 11, 2005
[Abdominal compartment syndrome: patophysiologic and clinic remarks]
F Stagnitti, S M Calderale, F Priore, et al.
Journal of Aging and Physical Activity
|
May 2, 2025
High-Intensity Functional Exercises Associated or Not With Cognitive Stimulation Improves Cognition and Physical Performance in Older Adults: A Double-Blind Randomized Controlled Trial
Enzo A R Teza, Felipe de S Stigger, Augusto Demarchi, et al.
American Journal of Human Genetics
|
April 1, 1996
An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p
J A Kaukonen, P Amati, A Suomalainen, et al.
Clinical Genetics
|
January 1, 1996
Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findings
A Ferlini, F Salvi, A Uncini, et al.
Human Mutation
|
January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis
M R Almeida, A Ferlini, A Forabosco, et al.
Page
of 15
Search research articles
Search
Showing results (101-110 of 146) with videos related to
Sort By:
Page
of 15
The Journal of Nutrition, Health & Aging
|
April 14, 2012
Screening for frailty in elderly emergency department patients by using the Identification of Seniors At Risk (ISAR)
F Salvi, V Morichi, A Grilli, et al.
Annals of Neurology
|
August 1, 1995
An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
M Ragno, E Tournier-Lasserve, M G Fiori, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 20, 2007
Brain structural damage in Friedreich's ataxia
R Della Nave, A Ginestroni, M Giannelli, et al.
Clinical Genetics
|
June 14, 2000
Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel hot spot' in codon 47
A Ferlini, L Obici, E Manzati, et al.
International Journal of Radiation Oncology, Biology, Physics
|
February 8, 2000
Radiation-induced gadd45 expression correlates with clinical response to radiotherapy of cervical carcinoma
M A Santucci, E Barbieri, G Frezza, et al.
Il Giornale Di Chirurgia
|
March 11, 2005
[Abdominal compartment syndrome: patophysiologic and clinic remarks]
F Stagnitti, S M Calderale, F Priore, et al.
Journal of Aging and Physical Activity
|
May 2, 2025
High-Intensity Functional Exercises Associated or Not With Cognitive Stimulation Improves Cognition and Physical Performance in Older Adults: A Double-Blind Randomized Controlled Trial
Enzo A R Teza, Felipe de S Stigger, Augusto Demarchi, et al.
American Journal of Human Genetics
|
April 1, 1996
An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p
J A Kaukonen, P Amati, A Suomalainen, et al.
Clinical Genetics
|
January 1, 1996
Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findings
A Ferlini, F Salvi, A Uncini, et al.
Human Mutation
|
January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis
M R Almeida, A Ferlini, A Forabosco, et al.
Page
of 15