Search research articles
Contact Us
Filters
Showing results (71-80 of 96) with videos related to
Page
of 10
Sort By:
Biochemical and Molecular Medicine
|
June 1, 1997
Expression study of survival motor neuron gene in human fetal tissues
G Novelli, L Calzà, P Amicucci, et al.
Bollettino Dell'Istituto Sieroterapico Milanese
|
January 1, 1990
Human neuronal cells in culture: from concepts to basic methodology
V Silani, A Pizzuti, M F Donato, et al.
Molecular Genetics and Metabolism
|
June 25, 1999
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome
A Pizzuti, G Novelli, A Ratti, et al.
Human Molecular Genetics
|
February 1, 1997
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome
A Pizzuti, G Novelli, A Ratti, et al.
Neuromuscular Disorders : NMD
|
May 23, 2001
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations
C Gellera, B Castellotti, M C Riggio, et al.
Neurology
|
August 26, 1998
A placebo-controlled trial of insulin-like growth factor-I in amyotrophic lateral sclerosis. European ALS/IGF-I Study Group
G D Borasio, W Robberecht, P N Leigh, et al.
Scientific Reports
|
June 25, 2020
Human salivary Raman fingerprint as biomarker for the diagnosis of Amyotrophic Lateral Sclerosis
C Carlomagno, P I Banfi, A Gualerzi, et al.
Acta Neurologica Scandinavica
|
May 15, 2013
Dysphagia in amyotrophic lateral sclerosis: prevalence and clinical findings
G Ruoppolo, I Schettino, V Frasca, et al.
Neurology
|
August 22, 2007
Phase II/III randomized trial of TCH346 in patients with ALS
R Miller, W Bradley, M Cudkowicz, et al.
The Neuroradiology Journal
|
September 25, 2013
Cerebral amyloid angiopathy-related inflammation: an emerging disease
M Savoiardo, A Erbetta, J C Di Francesco, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 96) with videos related to
Sort By:
Page
of 10
Biochemical and Molecular Medicine
|
June 1, 1997
Expression study of survival motor neuron gene in human fetal tissues
G Novelli, L Calzà, P Amicucci, et al.
Bollettino Dell'Istituto Sieroterapico Milanese
|
January 1, 1990
Human neuronal cells in culture: from concepts to basic methodology
V Silani, A Pizzuti, M F Donato, et al.
Molecular Genetics and Metabolism
|
June 25, 1999
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome
A Pizzuti, G Novelli, A Ratti, et al.
Human Molecular Genetics
|
February 1, 1997
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome
A Pizzuti, G Novelli, A Ratti, et al.
Neuromuscular Disorders : NMD
|
May 23, 2001
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations
C Gellera, B Castellotti, M C Riggio, et al.
Neurology
|
August 26, 1998
A placebo-controlled trial of insulin-like growth factor-I in amyotrophic lateral sclerosis. European ALS/IGF-I Study Group
G D Borasio, W Robberecht, P N Leigh, et al.
Scientific Reports
|
June 25, 2020
Human salivary Raman fingerprint as biomarker for the diagnosis of Amyotrophic Lateral Sclerosis
C Carlomagno, P I Banfi, A Gualerzi, et al.
Acta Neurologica Scandinavica
|
May 15, 2013
Dysphagia in amyotrophic lateral sclerosis: prevalence and clinical findings
G Ruoppolo, I Schettino, V Frasca, et al.
Neurology
|
August 22, 2007
Phase II/III randomized trial of TCH346 in patients with ALS
R Miller, W Bradley, M Cudkowicz, et al.
The Neuroradiology Journal
|
September 25, 2013
Cerebral amyloid angiopathy-related inflammation: an emerging disease
M Savoiardo, A Erbetta, J C Di Francesco, et al.
Page
of 10