Search details
1.
Factors influencing disease phenotype and penetrance in HFE haemochromatosis.
Hum Genet
; 128(3): 233-48, 2010 Sep.
Article
in English
| MEDLINE | ID: mdl-20607553
2.
Role of bioclimate conditions on cerebral aneurysm rupture in the Brittany region of France.
Neurochirurgie
; 66(1): 9-15, 2020 Feb.
Article
in English
| MEDLINE | ID: mdl-31836487
3.
Tuning of an active photonic crystal cavity by an hybrid silica/silicon near-field probe.
Opt Express
; 17(24): 21672-9, 2009 Nov 23.
Article
in English
| MEDLINE | ID: mdl-19997408
4.
Deciphering the molecular basis of ferroportin resistance to hepcidin: Structure/function analysis of rare SLC40A1 missense mutations found in suspected hemochromatosis type 4 patients.
Transfus Clin Biol
; 24(4): 462-467, 2017 Nov.
Article
in English
| MEDLINE | ID: mdl-28826751
5.
[Relevance of circulating tumor DNA in lung cancer: A case report]. / Intérêt de l'ADN tumoral circulant dans le cancer pulmonaire : à propos d'un cas.
Rev Mal Respir
; 33(9): 804-807, 2016 Nov.
Article
in French
| MEDLINE | ID: mdl-27132215
6.
Extracorporeal circuit for Panton-Valentine leukocidin-producing Staphylococcus aureus necrotizing pneumonia.
Med Mal Infect
; 46(6): 314-7, 2016 Sep.
Article
in English
| MEDLINE | ID: mdl-27210282
7.
Early-onset haemochromatosis caused by a novel combination of TFR2 mutations(p.R396X/c.1538-2 A>G) in a woman of Italian descent.
Haematologica
; 93(5): e45-6, 2008 May.
Article
in English
| MEDLINE | ID: mdl-18450729
8.
[Hepatic mucormycosis due to Rhizopus microsporus: A case report]. / Mucormycose hépatique à Rhizopus microsporus : description d'un cas.
Med Mal Infect
; 47(7): 504-507, 2017 11.
Article
in French
| MEDLINE | ID: mdl-28919389
9.
Variation of iron loading expression in C282Y homozygous haemochromatosis probands and sib pairs.
J Med Genet
; 38(9): 632-6, 2001 Sep.
Article
in English
| MEDLINE | ID: mdl-11565552
10.
Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC.
Clin Chem
; 47(9): 1633-40, 2001 Sep.
Article
in English
| MEDLINE | ID: mdl-11514397
11.
Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent.
Br J Haematol
; 125(5): 674-8, 2004 Jun.
Article
in English
| MEDLINE | ID: mdl-15147384
12.
Nramp2 analysis in hemochromatosis probands.
Blood Cells Mol Dis
; 26(4): 312-9, 2000 Aug.
Article
in English
| MEDLINE | ID: mdl-11042033
13.
Relation between HFE mutations and mild iron-overload expression.
Mol Genet Metab
; 69(4): 295-301, 2000 Apr.
Article
in English
| MEDLINE | ID: mdl-10870847
14.
Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada).
Br J Haematol
; 108(4): 854-8, 2000 Mar.
Article
in English
| MEDLINE | ID: mdl-10792295
15.
Clinical and molecular aspects of juvenile hemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, canada).
Blood Cells Mol Dis
; 26(1): 10-4, 2000 Feb.
Article
in English
| MEDLINE | ID: mdl-10772871
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