(Q50631474)

16 March 2018

review article

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title

[Genetic causes of impaired wound healing. Rare differential diagnosis of the non-healing wound]. (English)

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16 March 2018

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K Elsharkawi-Welt

1

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16 March 2018

J Hepp

series ordinal

2

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16 March 2018

K Scharffetter-Kochanek

series ordinal

3

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16 March 2018

language of work or name

German

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publication date

1 November 2008

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16 March 2018

published in

Die Dermatologie

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16 March 2018

volume

59

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16 March 2018

issue

11

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16 March 2018

page(s)

893-903

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16 March 2018

https://scigraph.springernature.com/pub.10.1007/s00105-008-1591-2

exact match

0 references

cites work

Total absence of the alpha2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problems.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00105-008-1591-2

Activated protein C resistance and thrombosis

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00105-008-1591-2

Clinical and immunological aspects of HLA class I deficiency.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00105-008-1591-2

21 January 2018

TAP deficiency syndrome

1 reference

12 December 2020

RecQ helicases: caretakers of the genome

1 reference

12 December 2020

Methylenetetrahydrofolate reductase polymorphism associated with moderate hyperhomocysteinaemia in a patient with livedo vasculopathy: treatment with vitamin supplementation and low molecular weight heparin

1 reference

12 December 2020

Ulcers of the leg in thalassemia

1 reference

12 December 2020

Reduction of the clinical severity of sickle cell/beta-thalassemia with hydroxyurea: the experience of a single center in Greece

1 reference

12 December 2020

Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase

1 reference

12 December 2020

INHERITED ANTITHROMBIN DEFICIENCY CAUSING THROMBOPHILIA

1 reference

12 December 2020

HLA class I deficiency syndrome mimicking Wegener's granulomatosis.

1 reference

12 December 2020

Leg ulcers in Klinefelter's syndrome--further evidence for an involvement of plasminogen activator inhibitor-1.

1 reference

12 December 2020

Homocysteine and hemostasis: pathogenic mechanisms predisposing to thrombosis

1 reference

12 December 2020

Leg ulceration in the sickle cell patient

1 reference

12 December 2020

Dystrophic Epidermolysis Bullosa Inversa with COL7A1 Mutations and Absence of GDA-J/F3 Protein

1 reference

12 December 2020

Hutchinson-Gilford progeria syndrome

1 reference

12 December 2020

Antigen degradation or presentation by MHC class I molecules via classical and non-classical pathways

1 reference

12 December 2020

Platelet hyperaggregability in two patients with Klinefelter's syndrome complicated by leg ulcers

1 reference

12 December 2020

Leukocyte adhesion deficiency II. Advances and open questions

1 reference

12 December 2020

Hematologically important mutations: leukocyte adhesion deficiency

1 reference

12 December 2020

Werner's syndrome as a cause of chronic leg ulcers

1 reference

12 December 2020

Predilection of hemolytic anemia-associated leg ulcers for the medial malleolus

1 reference

12 December 2020

Discontinuation of fucose therapy in LADII causes rapid loss of selectin ligands and rise of leukocyte counts

1 reference

12 December 2020

Sickle cell anaemia: progress in pathogenesis and treatment

1 reference

12 December 2020

Leukocyte Adhesion Deficiency Type II is a generalized defect of de novo GDP-fucose biosynthesis. Endothelial cell fucosylation is not required for neutrophil rolling on human nonlymphoid endothelium

1 reference

12 December 2020

Treatment of sickle cell leg ulcers with pentoxifylline

1 reference

12 December 2020

Wound-healing defect of CD18(-/-) mice due to a decrease in TGF-beta1 and myofibroblast differentiation

1 reference

12 December 2020

Plasma protein S deficiency in familial thrombotic disease

1 reference

12 December 2020

Plasminogen activator inhibitor in plasma is related to testosterone in men

1 reference

12 December 2020

Management of sickle cell disease.

1 reference

12 December 2020

Deficiency of protein C in congenital thrombotic disease

1 reference

12 December 2020

The role of hydroxyurea in sickle cell disease.

1 reference

12 December 2020

Leukocyte adhesion deficiency: an inherited defect in the Mac-1, LFA-1, and p150,95 glycoproteins

1 reference

12 December 2020

Spontaneous skin ulceration and defective T cell function in CD18 null mice

1 reference

12 December 2020

Leukocyte adhesion deficiency: clinical and postmortem observations

1 reference

12 December 2020

LAD-III, a novel group of leukocyte integrin activation deficiencies.

1 reference

12 December 2020

Increased activity of factor VIII coagulant associated with venous ulcer in a patient with Klinefelter's syndrome

1 reference

12 December 2020

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.

1 reference

12 December 2020

Leukocyte adhesion deficiency II patients with a dual defect of the GDP-fucose transporter

1 reference

12 December 2020

Venous thromboembolic disease in Klinefelter's syndrome

1 reference

12 December 2020

Dermatomyositis responding to pentoxifylline

1 reference

12 December 2020

An initiation codon mutation in CD18 in association with the moderate phenotype of leukocyte adhesion deficiency.

1 reference

12 December 2020

Genetics and immunopathology of chronic granulomatous disease

1 reference

12 December 2020

10.1007/S00105-008-1591-2

Identifiers

DOI

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16 March 2018

1 reference

16 March 2018