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Inherited plasminogen deficiency presenting as ligneous vaginitis: a case report with molecular correlation and review of the literature

Human pathology, 2007-10, Vol.38 (10), p.1569-1575

2007

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Ligneous inflammation involving the female genital tract

The journal of obstetrics and gynaecology research, 2007-08, Vol.33 (4), p.581-584

2007

Volltextzugriff (PDF)

Characterization of plasminogen variants in healthy subjects and plasminogen mutants in patients with inherited plasminogen deficiency by isoelectric focusing gel electrophoresis

Thrombosis and haemostasis, 2004-08, Vol.92 (2), p.352

2004

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Transcriptional regulation of the human KiSS1 gene

Molecular and cellular endocrinology, 2011-08, Vol.342 (1), p.8-19

2011

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Estrogen modulates plasminogen promoter activity

Biochemical and biophysical research communications, 2013-08, Vol.438 (1), p.110-115

2013

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Duodenal ulceration in a patient with celiac disease and plasminogen I deficiency: coincidence or cofactors?

Pediatrics (Evanston), 2011-11, Vol.128 (5), p.e1302

2011

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Hypoplasminogenemia With Ligneous Periodontitis: A Failed Local Therapeutic Approach

Journal of periodontology (1970), 2007-06, Vol.78 (6), p.1164-1175

2007

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Transcriptional Regulation of the Human Gene

Molecular and cellular endocrinology, 2011-07, Vol.342 (1-2)

2011

Volltextzugriff (PDF)

Isoelectric focusing pattern of plasminogen mutants of patients with hypoplasminogenemia: correlation of in-vitro data with computer-predicted isoelectric points (pI)

Blood coagulation & fibrinolysis, 2011-09, Vol.22 (6), p.499-505

2011

Volltextzugriff (PDF)

Therapeutic approaches in the treatment of ligneous conjunctivitis, the most common clinical manifestation of a systemic disease, caused by severe type I plasminogen deficiency

American journal of ophthalmology, 2004-10, Vol.138 (4), p.699-699

2004

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Ligneous conjunctivitis, hydrocephalus, hydrocele, and pulmonary involvement in a child with homozygous type I plasminogen deficiency

European journal of pediatrics, 2003-07, Vol.162 (7-8), p.462-465

2003

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Ligneous (Pseudomembranous) Inflammation Involving the Female Genital Tract Associated with Type-1 Plasminogen Deficiency

International journal of gynecological pathology, 2004-07, Vol.23 (3), p.292-295

2004

Volltextzugriff (PDF)

A nucleic acid exchange in Intron F (Intron F-14T>G) in the human plasminogen gene is only a common polymorphism and not a true mutation

Thrombosis and haemostasis, 2004-04, Vol.91 (4), p.830

2004

Volltextzugriff (PDF)

A K19E missense mutation in the plasminogen gene is a common cause of familial hypoplasminogenaemia

Blood coagulation & fibrinolysis, 2003-06, Vol.14 (4), p.411-416

2003

Volltextzugriff (PDF)

Difficulties in mutation screening of the plasminogen (PLG) gene in patients with ligneous conjunctivitis and severe hypoplasminogenemia

Archives of ophthalmology (1960), 2007-09, Vol.125 (9), p.1303; author reply 1303

2007

Volltextzugriff (PDF)

Ligneous inflammation involving the female genital tract

Journal of Obstetrics and Gynaecology Research, 2007, Vol.33 (4), p.581-584

2007

Volltextzugriff (PDF)

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Inherited plasminogen deficiency presenting as ligneous vaginitis: a case report with molecular correlation and review of the literature

Ligneous inflammation involving the female genital tract

Characterization of plasminogen variants in healthy subjects and plasminogen mutants in patients with inherited plasminogen deficiency by isoelectric focusing gel electrophoresis

Transcriptional regulation of the human KiSS1 gene

Estrogen modulates plasminogen promoter activity

Duodenal ulceration in a patient with celiac disease and plasminogen I deficiency: coincidence or cofactors?

Hypoplasminogenemia With Ligneous Periodontitis: A Failed Local Therapeutic Approach

Transcriptional Regulation of the Human Gene

Isoelectric focusing pattern of plasminogen mutants of patients with hypoplasminogenemia: correlation of in-vitro data with computer-predicted isoelectric points (pI)

Therapeutic approaches in the treatment of ligneous conjunctivitis, the most common clinical manifestation of a systemic disease, caused by severe type I plasminogen deficiency

Ligneous conjunctivitis, hydrocephalus, hydrocele, and pulmonary involvement in a child with homozygous type I plasminogen deficiency

Ligneous (Pseudomembranous) Inflammation Involving the Female Genital Tract Associated with Type-1 Plasminogen Deficiency

A nucleic acid exchange in Intron F (Intron F-14T>G) in the human plasminogen gene is only a common polymorphism and not a true mutation

A K19E missense mutation in the plasminogen gene is a common cause of familial hypoplasminogenaemia

Difficulties in mutation screening of the plasminogen (PLG) gene in patients with ligneous conjunctivitis and severe hypoplasminogenemia

Ligneous inflammation involving the female genital tract

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