author-photo

Franco Martinez di Montemuros

University of Milan

12

Papers

225

Citations

Citation Trend

Filter By

Papers (12) Sort By

Journal Conference Others

Molecular characterisation of an Italian G6PD variant responsible for chronic non-spherocytic haemolytic anaemia

2008 Clinical Genetics
Show All
- Source
- Cite
- Save
Citations (4)
Hematologically important mutations: acute intermittent porphyria.

2002 Blood Cells Molecules and Diseases
Show All
- Source
- Cite
- Save
Citations (11)
Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian population.

2000 Hematology Journal
Show All
- Source
- Cite
- Save
Citations (16)
Molecular Analysis of the Hydroxymethylbilane Synthase (HMBS) Gene in Italian Patients with Acute Intermittent Porphyria: Report of Four Novel Mutations

2000 Human Mutation
Show All
- Source
- Cite
- Save
Citations (16)
A novel polymorphism (219G>A) in the transferrin receptor gene.

2000 Human Mutation
Show All
- Source
- Cite
- Save
Citations (2)
Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants

2000 Best Practice & Research Clinical Haematology
Show All
- Source
- Cite
- Save
Citations (45)
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency.

1997 British Journal of Haematology
Show All
- Source
- Cite
- Save
Citations (92)
Molecular characterisation of the glucose-6-phosphate dehydrogenase (G6PD) Ferrara II variant

1995 Human Genetics
Show All
- Source
- Cite
- Save
Citations (7)
Biochemical and molecular characterization of a new sporadic glucose-6-phosphate dehydrogenase variant described in Italy: G6PD Modena

1994 British Journal of Haematology
Show All
- Source
- Cite
- Save
Citations (6)
G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype

1994 Human Genetics
Show All
- Source
- Cite
- Save
Citations (14)