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Biochemical and Biophysical Research Communications
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February 3, 1998
The 5' region of intron 11 of the dystrophin gene contains target sequences for mobile elements and three overlapping ORFs
A Ferlini, F Muntoni
Annali Sclavo; Rivista Di Microbiologia E Di Immunologia
|
July 1, 1973
[Urinary tract infections in patients hospitalized in a department of internal medicine. Bacteriological and clinical studies and therapeutic results in 925 cases]
A Visani, A Ferlini
Orphanet Journal of Rare Diseases
|
February 11, 2021
Survey on patients' organisations' knowledge and position paper on screening for inherited neuromuscular diseases in Europe
F Lamy, A Ferlini, , et al.
Minerva Pediatrica
|
August 31, 1986
[New instruments in molecular genetics for the prevention of X chromosome-linked muscular dystrophy]
A Ferlini, L Roncuzzi, G Romeo
Public Health Genomics
|
February 8, 2014
Biomarkers in rare diseases
A Ferlini, C Scotton, G Novelli
European Journal of Epidemiology
|
April 13, 2002
Epidemiological survey of X-linked bulbar and spinal muscular atrophy, or Kennedy disease, in the province of Reggio Emilia, Italy
D Guidetti, R Sabadini, A Ferlini, et al.
Human Genetics
|
December 1, 1986
Origin of new mutations in Duchenne muscular dystrophy
L Roncuzzi, A Ferlini, A Pirozzi, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1986
Rett syndrome: lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations
G Romeo, N Archidiacono, A Ferlini, et al.
American Journal of Medical Genetics
|
September 1, 1991
Reduced activity of arylsulfatase A and predisposition to neurological disorders: analysis of 140 pediatric patients
S Sangiorgi, A Ferlini, A Zanetti, et al.
Giornale Di Clinica Medica
|
November 1, 1990
[Clinical case. Metastatic pulmonary microcytoma]
G Marano, G Marchi, T Fabbri, et al.
Page
of 9
Search research articles
Search
Showing results (1-10 of 88) with videos related to
Sort By:
Page
of 9
Biochemical and Biophysical Research Communications
|
February 3, 1998
The 5' region of intron 11 of the dystrophin gene contains target sequences for mobile elements and three overlapping ORFs
A Ferlini, F Muntoni
Annali Sclavo; Rivista Di Microbiologia E Di Immunologia
|
July 1, 1973
[Urinary tract infections in patients hospitalized in a department of internal medicine. Bacteriological and clinical studies and therapeutic results in 925 cases]
A Visani, A Ferlini
Orphanet Journal of Rare Diseases
|
February 11, 2021
Survey on patients' organisations' knowledge and position paper on screening for inherited neuromuscular diseases in Europe
F Lamy, A Ferlini, , et al.
Minerva Pediatrica
|
August 31, 1986
[New instruments in molecular genetics for the prevention of X chromosome-linked muscular dystrophy]
A Ferlini, L Roncuzzi, G Romeo
Public Health Genomics
|
February 8, 2014
Biomarkers in rare diseases
A Ferlini, C Scotton, G Novelli
European Journal of Epidemiology
|
April 13, 2002
Epidemiological survey of X-linked bulbar and spinal muscular atrophy, or Kennedy disease, in the province of Reggio Emilia, Italy
D Guidetti, R Sabadini, A Ferlini, et al.
Human Genetics
|
December 1, 1986
Origin of new mutations in Duchenne muscular dystrophy
L Roncuzzi, A Ferlini, A Pirozzi, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1986
Rett syndrome: lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations
G Romeo, N Archidiacono, A Ferlini, et al.
American Journal of Medical Genetics
|
September 1, 1991
Reduced activity of arylsulfatase A and predisposition to neurological disorders: analysis of 140 pediatric patients
S Sangiorgi, A Ferlini, A Zanetti, et al.
Giornale Di Clinica Medica
|
November 1, 1990
[Clinical case. Metastatic pulmonary microcytoma]
G Marano, G Marchi, T Fabbri, et al.
Page
of 9