Found: 14
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Results of an Ophthalmologic Screening Programme for Identification of Cases with Anderson-Fabry Disease.
- Published in:
- Ophthalmologica, 2004, v. 218, n. 3, p. 207, doi. 10.1159/000076846
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- Publication type:
- Article
High prevalence of subclinical hypothyroidism in patients with Anderson–Fabry disease.
- Published in:
- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 5, p. 715, doi. 10.1007/s10545-005-0003-3
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- Publication type:
- Article
Comorbidity, iron overload and HFE variants: a new prognostic complex in MDS?
- Published in:
- 2009
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- Publication type:
- Letter
Mixed-lineage eosinophil/basophil crisis in MDS: a rare form of progression.
- Published in:
- European Journal of Clinical Investigation, 2008, v. 38, n. 6, p. 447, doi. 10.1111/j.1365-2362.2008.01950.x
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- Publication type:
- Article
Immunohistochemical assessment of CD25 is equally sensitive and diagnostic in mastocytosis compared to flow cytometry.
- Published in:
- European Journal of Clinical Investigation, 2008, v. 38, n. 5, p. 326, doi. 10.1111/j.1365-2362.2008.01942.x
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- Publication type:
- Article
Standards and standardization in mastocytosis: Consensus Statements on Diagnostics, Treatment Recommendations and Response Criteria.
- Published in:
- European Journal of Clinical Investigation, 2007, v. 37, n. 6, p. 435, doi. 10.1111/j.1365-2362.2007.01807.x
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- Publication type:
- Article
Granulocyte function in patients with L-ferritin iron-responsive element (IRE) 39C→T-positive hereditary hyperferritinaemia–cataract syndrome.
- Published in:
- European Journal of Clinical Investigation, 2004, v. 34, n. 10, p. 701, doi. 10.1111/j.1365-2362.2004.01408.x
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- Publication type:
- Article
Patterns of co-occurrence of three single nucleotide polymorphisms of the 5,10-methylenetetrahydrofolate reductase gene in kidney transplant recipients.
- Published in:
- European Journal of Clinical Investigation, 2004, v. 34, n. 9, p. 613, doi. 10.1111/j.1365-2362.2004.01394.x
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- Publication type:
- Article
Low clinical penetrance of homozygosity for HFE C282Y: implications for genetic testing?
- Published in:
- 2003
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- Publication type:
- Editorial
Numbers of colony-forming progenitors in patients with systemic mastocytosis: potential diagnostic implications and comparison with myeloproliferative disorders.
- Published in:
- European Journal of Clinical Investigation, 2003, v. 33, n. 7, p. 611, doi. 10.1046/j.1365-2362.2003.01172.x
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- Publication type:
- Article
Schlaganfall bei Tumorpatienten.
- Published in:
- Der Nervenarzt, 2010, v. 81, n. 4, p. 418, doi. 10.1007/s00115-010-2952-5
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- Publication type:
- Article
Hyperfibrinolysis in a case of myelodysplastic syndrome with leukemic spread of mast cells.
- Published in:
- American Journal of Hematology, 1999, v. 61, n. 1, p. 66, doi. 10.1002/(SICI)1096-8652(199905)61:1<66::AID-AJH12>3.0.CO;2-3
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- Publication type:
- Article
Resistance to activated protein C (APC): mutation at ARG506 of coagulation factor V and vascular access thrombosis in haemodialysis patients.
- Published in:
- Nephrology Dialysis Transplantation, 1996, v. 11, n. 4, p. 668, doi. 10.1093/oxfordjournals.ndt.a027357
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- Publication type:
- Article
Photodegradation of folic acid during extracorporeal photopheresis.
- Published in:
- British Journal of Dermatology, 2007, v. 156, n. 1, p. 117, doi. 10.1111/j.1365-2133.2006.07569.x
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- Publication type:
- Article