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A Fogli

Showing results (11-20 of 35) with videos related to

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Biochemical Society Transactions|October 26, 2005
The large spectrum of eIF2B-related diseasesA Fogli, O Boespflug-Tanguy
Annales De Biologie Clinique|November 28, 2007
[Monoclonal IgM interference with immunoturbidimetric determination of ferritin and transferrin]L Roszyk, B Faye, O Tournilhac, et al.
Genomics|August 7, 1998
The beta and gamma subunits of the human platelet-activating factor acetyl hydrolase isoform Ib (PAFAH1B2 and PAFAH1B3) map to chromosome 11q23 and 19q13.1, respectivelyF Moro, G Arrigo, A Fogli, et al.
Revue Neurologique|September 20, 2007
[CACH/VWM syndrome and leucodystrophies related to EIF2B mutations]P Labauge, A Fogli, F Niel, et al.
Journal Francais D'Oto-Rhino-Laryngologie, Audio-Phonologie Et Chirurgie Maxillo-Faciale|November 1, 1971
[Contribution of microlaryngoscopy to the detection of precancerous states and beginning laryngeal cancers]A Pech, Y Borrot, S Cahier, et al.
Professioni Infermieristiche|January 1, 1975
[Psychiatric activities: report of the first year's activities (3-1-72 - 3-1-73) of of the work of Sector V, West Turin]G Zirillo, A Fogli, G Tribbioli, et al.
Annals of Human Genetics|February 26, 2008
Exon deletion in the non-catalytic domain of eIF2Bepsilon due to a splice site mutation leads to infantile forms of CACH/VWM with severe decrease of eIF2B GEF activityL Horzinski, C Gonthier, D Rodriguez, et al.
Contributions to Nephrology|November 2, 2001
Nonsense mutation in exon 2 of the alpha-galactosidase A gene in a patient with Fabry diseaseE Manni, A Fogli, F Baldinotti, et al.
Neurology|December 25, 2002
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutationA Fogli, C Dionisi-Vici, F Deodato, et al.
Minerva Anestesiologica|June 12, 2013
Comparison of three methods of diagnosis of plasma unmeasured anions in critically ill patientsA Lautrette, M Fejjal, A Aithssain, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Biochemical Society Transactions|October 26, 2005
The large spectrum of eIF2B-related diseasesA Fogli, O Boespflug-Tanguy
Annales De Biologie Clinique|November 28, 2007
[Monoclonal IgM interference with immunoturbidimetric determination of ferritin and transferrin]L Roszyk, B Faye, O Tournilhac, et al.
Genomics|August 7, 1998
The beta and gamma subunits of the human platelet-activating factor acetyl hydrolase isoform Ib (PAFAH1B2 and PAFAH1B3) map to chromosome 11q23 and 19q13.1, respectivelyF Moro, G Arrigo, A Fogli, et al.
Revue Neurologique|September 20, 2007
[CACH/VWM syndrome and leucodystrophies related to EIF2B mutations]P Labauge, A Fogli, F Niel, et al.
Journal Francais D'Oto-Rhino-Laryngologie, Audio-Phonologie Et Chirurgie Maxillo-Faciale|November 1, 1971
[Contribution of microlaryngoscopy to the detection of precancerous states and beginning laryngeal cancers]A Pech, Y Borrot, S Cahier, et al.
Professioni Infermieristiche|January 1, 1975
[Psychiatric activities: report of the first year's activities (3-1-72 - 3-1-73) of of the work of Sector V, West Turin]G Zirillo, A Fogli, G Tribbioli, et al.
Annals of Human Genetics|February 26, 2008
Exon deletion in the non-catalytic domain of eIF2Bepsilon due to a splice site mutation leads to infantile forms of CACH/VWM with severe decrease of eIF2B GEF activityL Horzinski, C Gonthier, D Rodriguez, et al.
Contributions to Nephrology|November 2, 2001
Nonsense mutation in exon 2 of the alpha-galactosidase A gene in a patient with Fabry diseaseE Manni, A Fogli, F Baldinotti, et al.
Neurology|December 25, 2002
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutationA Fogli, C Dionisi-Vici, F Deodato, et al.
Minerva Anestesiologica|June 12, 2013
Comparison of three methods of diagnosis of plasma unmeasured anions in critically ill patientsA Lautrette, M Fejjal, A Aithssain, et al.
Pageof 4