C Camaschella
Overview
Explore the profile of C Camaschella including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
141
Citations
1054
Followers
0
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Recent Articles
1.
Bordini J, Galvan S, Ponzoni M, Bertilaccio M, Chesi M, Bergsagel P, et al.
Leukemia
. 2016 Nov;
31(4):967-970.
PMID: 27881873
No abstract available.
2.
Piacibello W, Camaschella C, Stern A, Aglietta M
Leuk Lymphoma
. 2016 Jul;
3(1):61-6.
PMID: 27457199
After several relapses, a stage IV lymphocyte depletion Hodgkin Lymphoma patient, with a bone marrow progenitor compartment depleted by several courses of chemotherapy, received further combination chemotherapy which caused severe...
3.
Camaschella C, Pagani A, Nai A, Silvestri L
Int J Lab Hematol
. 2016 May;
38 Suppl 1:20-6.
PMID: 27161430
Background: Iron is essential for hemoglobin synthesis during terminal erythropoiesis. To supply adequate iron the carrier transferrin is required together with transferrin receptor endosomal cycle and normal mitochondrial iron utilization....
4.
Orlandi R, De Bortoli M, Ciniselli C, Vaghi E, Caccia D, Garrisi V, et al.
Ann Oncol
. 2013 Dec;
25(2):352-7.
PMID: 24306042
Background: Currently used CA15-3 and CEA have found their clinical application particularly in the follow-up of patients with advanced disease. Novel biomarkers are urgent, especially for improving early diagnosis as...
5.
Iolascon A, Camaschella C, Pospisilova D, Piscopo C, Tchernia G, Beaumont C
J Pediatr
. 2007 Dec;
152(1):136-9.
PMID: 18154916
DMT1 deficiency causes microcytic hypochromic anemia due to decreased erythroid iron utilization. Anemia is present from birth. Transferrin saturation is high and serum ferritin is mildly elevated, despite liver iron...
6.
Camaschella C, Merlini R
Minerva Med
. 2005 Sep;
96(3):207-22.
PMID: 16175162
Hereditary hemochromatosis is one of the most common autosomal recessive disorder among Caucasians since the genotype at risk for hemochromatosis accounts for 1:200-400 individuals of Northern European ancestry. The disease...
7.
Daraio F, Ryan E, Gleeson F, Roetto A, Crowe J, Camaschella C
Blood Cells Mol Dis
. 2005 Jun;
35(2):174-6.
PMID: 15967692
Hemojuvelin (HJV) is a recently discovered gene responsible for 1q-linked juvenile hemochromatosis. The majority of mutations characterized in this gene are rare and private, except G320V, identified in patients from...
8.
De Gobbi M, Caruso R, Daraio F, Chianale F, Pinto R, Longo F, et al.
Eur J Pediatr
. 2003 Jan;
162(2):96-9.
PMID: 12548385
Unlabelled: Juvenile or type2 hemochromatosis is a rare autosomal recessive disorder which leads to severe iron overload early in life. As in the classic adult form of the disease iron...
9.
Papanikolaou G, Politou M, Roetto A, Bosio S, Sakelaropoulos N, Camaschella C, et al.
Blood Cells Mol Dis
. 2002 Jan;
27(4):744-9.
PMID: 11778658
Hereditary hemochromatosis (HH) is a genetically heterogeneous disease. The HFE gene resides on chromosome 6 and its mutations account for the majority of HH cases in populations of northern European...
10.
Girelli D, Bozzini C, Zecchina G, Tinazzi E, Bosio S, Piperno A, et al.
Br J Haematol
. 2001 Nov;
115(2):334-40.
PMID: 11703332
Hereditary hyperferritinaemia-cataract syndrome (HHCS) is an autosomal dominant disease caused by mutations in the iron responsive element (IRE) of the l-ferritin gene. Despite the elucidation of the genetic basis, the...