Sfoglia per AUTORE
CAMASCHELLA C
Collezione AOU San Luigi di Orbassano

  

Items : 20

Reactive thrombocytosis might contribute to chemotherapy-related thrombophilia in patients with lung cancer. in Clinical lung cancer / Clin Lung Cancer. 2007 Jan;8(4):264-7. doi: 10.3816/CLC.2007.n.004.
2007
AOU San Luigi di Orbassano

Zecchina G; Ghio P; Bosio S; Cravino M; Camaschella C; Scagliotti GV;

Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patient. in Blood cells, molecules & diseases / Blood Cells Mol Dis. 2005 Sep-Oct;35(2):174-6. doi: 10.1016/j.bcmd.2005.02.001.
2005
AOU San Luigi di Orbassano

Daraio F; Ryan E; Gleeson F; Roetto A; Crowe J; Camaschella C;

2005
AOU San Luigi di Orbassano

Bondi A; Valentino P; Daraio F; Porporato P; Gramaglia E; Carturan S; Gottardi E; Camaschella C; Roetto A;

New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis. in Best practice & research. Clinical haematology / Best Pract Res Clin Haematol. 2005 Jun;18(2):235-50. doi: 10.1016/j.beha.2004.09.004.
2005
AOU San Luigi di Orbassano

Roetto A; Camaschella C;

Inherited hemochromatosis: from genetics to clinics. in Minerva medica / Minerva Med. 2005 Jun;96(3):207-22.
2005
AOU San Luigi di Orbassano

Camaschella C; Merlini R;

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis. in Nature genetics / Nat Genet. 2003 Jan;33(1):21-2. doi: 10.1038/ng1053. Epub 2002 Dec 9.
2003
AOU San Luigi di Orbassano

Roetto A; Papanikolaou G; Politou M; Alberti F; Girelli D; Christakis J; Loukopoulos D; Camaschella C;

Diagnosis of juvenile hemochromatosis in an 11-year-old child combining genetic analysis and non-invasive liver iron quantitation. in European journal of pediatrics / Eur J Pediatr. 2003 Feb;162(2):96-9. doi: 10.1007/s00431-002-1114-6. Epub 2002 Dec 10.
2003
AOU San Luigi di Orbassano

De Gobbi M; Caruso R; Daraio F; Chianale F; Pinto RM; Longo F; Piga A; Camaschella C;

Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations. in Blood / Blood. 2002 Sep 15;100(6):2246-8. doi: 10.1182/blood-2002-02-0584.
2002
AOU San Luigi di Orbassano

Bosio S; De Gobbi M; Roetto A; Zecchina G; Leonardo E; Rizzetto M; Lucetti C; Petrozzi L; Bonuccelli U; Camaschella C;

Hemochromatosis due to mutations in transferrin receptor 2. in Blood cells, molecules & diseases / Blood Cells Mol Dis. 2002 Nov-Dec;29(3):465-70. doi: 10.1006/bcmd.2002.0585.
2002
AOU San Luigi di Orbassano

Roetto A; Daraio F; Alberti F; Porporato P; Calì A; De Gobbi M; Camaschella C;

Pathogenesis of hyperferritinemia cataract syndrome. in Blood cells, molecules & diseases / Blood Cells Mol Dis. 2002 Nov-Dec;29(3):532-5. doi: 10.1006/bcmd.2002.0590.
2002
AOU San Luigi di Orbassano

Roetto A; Bosio S; Gramaglia E; Barilaro MR; Zecchina G; Camaschella C;

Natural history of juvenile haemochromatosis. in British journal of haematology / Br J Haematol. 2002 Jun;117(4):973-9. doi: 10.1046/j.1365-2141.2002.03509.x.
2002
AOU San Luigi di Orbassano

De Gobbi M; Roetto A; Piperno A; Mariani R; Alberti F; Papanikolaou G; Politou M; Lockitch G; Girelli D; Fargion S; Cox TM; Gasparini P; Cazzola M; Camaschella C;

Genetic haemochromatosis: genes and mutations associated with iron loading. in Best practice & research. Clinical haematology / Best Pract Res Clin Haematol. 2002 Jun;15(2):261-76. doi: 10.1016/s1521-6926(02)90207-0.
2002
AOU San Luigi di Orbassano

Camaschella C; Roetto A; De Gobbi M;

Commentary: Juvenile hemochromatosis in a Spanish family (by Montes-Cano et al.). in Blood cells, molecules & diseases / Blood Cells Mol Dis. 2002 Jul-Aug;29(1):83-4; author reply 85. doi: 10.1006/bcmd.2002.0543.
2002
AOU San Luigi di Orbassano

Camaschella C; Roetto A; Papanikolaou G;

New mutations inactivating transferrin receptor 2 in hemochromatosis type 3. in Blood / Blood. 2001 May 1;97(9):2555-60. doi: 10.1182/blood.v97.9.2555.
2001
AOU San Luigi di Orbassano

Roetto A; Totaro A; Piperno A; Piga A; Longo F; Garozzo G; Calì A; De Gobbi M; Gasparini P; Camaschella C;

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22. in Nature genetics / Nat Genet. 2000 May;25(1):14-5. doi: 10.1038/75534.
2000
AOU San Luigi di Orbassano

Camaschella C; Roetto A; Calì A; De Gobbi M; Garozzo G; Carella M; Majorano N; Totaro A; Gasparini P;

Exclusion of ZIRTL as candidate gene of juvenile hemochromatosis and refinement of the critical interval on 1q21. in Blood cells, molecules & diseases / Blood Cells Mol Dis. 2000 Jun;26(3):205-10. doi: 10.1006/bcmd.2000.0297.
2000
AOU San Luigi di Orbassano

Roetto A; Alberti F; Daraio F; Cali A; Cazzola M; Totaro A; Gasparini P; Camaschella C;

1999
AOU San Luigi di Orbassano

Cicilano M; Zecchina G; Roetto A; Bosio S; Infelise V; Stefani S; Mazza U; Camaschella C;

Feasibility of molecular diagnosis of alpha-thalassemia in the evaluation of microcytosis. in Haematologica / Haematologica. 1997 Sep-Oct;82(5):592-3.
1997
AOU San Luigi di Orbassano

Sivera P; Roetto A; Mazza U; Camaschella C;

Hereditary hemochromatosis: recent advances in molecular genetics and clinical management. in Haematologica / Haematologica. 1997 Jan-Feb;82(1):77-84.
1997
AOU San Luigi di Orbassano

Camaschella C; Piperno A;

A frequent polymorphism in the 5' region of the BCMA gene. in Molecular and cellular probes / Mol Cell Probes. 1997 Aug;11(4):311-2. doi: 10.1006/mcpr.1997.0115.
1997
AOU San Luigi di Orbassano

Roetto A; Cicilano M; Gottardi E; Totaro A; Carella M; Gasparini P; Camaschella C;

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