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SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q

Neurology, 2001-05, Vol.56 (9), p.1230

2001

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Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutations

Neurology, 2000-12, Vol.55 (12), p.1794

2000

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Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p

Neurology, 2000-04, Vol.54 (7), p.1510

2000

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bcl-2 protein expression is associated with better prognosis in colorectal cancer

Histopathology, 1999-10, Vol.35 (4), p.360-367

1999

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Expansion of peripheral blood CD5 + B cells is associated with mild disease in chronic hepatitis C virus infection

Journal of hepatology, 2000, Vol.32 (1), p.121-125

2000

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Post-transplant lymphoproliferative disorder in renal allograft recipients. Clinical experience and risk factor analysis in a single center

Transplantation, 1993-07, Vol.56 (1), p.88

1993

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Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct

British journal of ophthalmology, 1999-01, Vol.83 (1), p.115-119

1999

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Localization of the Gene for Autosomal Recessive Congenital Hereditary Endothelial Dystrophy (CHED2) to Chromosome 20 by Homozygosity Mapping

Genomics (San Diego, Calif.), 1999-10, Vol.61 (1), p.1-4

1999

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Increased major histocompatibility complex antigen expression in unilateral ischemic acute tubular necrosis in the mouse

Transplantation, 1990-01, Vol.49 (1), p.201

1990

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PROGNOSTIC SIGNIFICANCE OF p53 ABNORMALITIES IN COLORECTAL CARCINOMA DETECTED BY PCR-SSCP AND IMMUNOHISTOCHEMICAL ANALYSIS

The Journal of pathology, 1996-12, Vol.180 (4), p.364-370

1996

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Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation

Neurology, 2001-01, Vol.56 (1), p.139

2001

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Effects of fenoldopam on renal blood flow and its function in a canine model of rhabdomyolysis

European journal of anaesthesiology, 2003-09, Vol.20 (9), p.711-718

2003

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Interferon-gamma gene expression during acute graft-versus-host disease: relationship to MHC induction and tissue injury

The Journal of pathology, 1999-09, Vol.189 (1), p.99-104

1999

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Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

Human molecular genetics, 2000-03, Vol.9 (4), p.637-644

2000

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Effects of fenoldopam on renal blood flow and its function in a canine model of rhabdomyolysis

European journal of anaesthesiology, 2003-09, Vol.20 (9), p.711-718

2003

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Squamous cell carcinoma arising in a skin graft donor site following melanoma extirpation at a distant site: A case report and review of the literature

JPRAS open, 2015-03, Vol.3 (C), p.35-38

2015

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Interferon gamma-mediated renal MHC expression in mercuric chloride-induced glomerulonephritis

Kidney international, 1991-02, Vol.39 (2), p.273-281

1991

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Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance

European journal of human genetics : EJHG, 1998-05, Vol.6 (3), p.275-282

1998

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The decreased incidence of aseptic necrosis in renal transplant recipients--a case control study

Transplantation, 1986-02, Vol.41 (2), p.182

1986

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Cyclosporine-Induced Autoimmunity and Immune Hyperreactivity

Autoimmunity (Chur, Switzerland), 1991, Vol.9 (4), p.345-356

1991

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In vitro cold activation of complement shown by an overestimation of total complement 4: a study in patients with hepatitis C virus infection

Annals of clinical biochemistry, 2001-11, Vol.38 (Pt 6), p.687

2001

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Patterns of MHC antigenic modulation in cyclosporine-induced autoimmunity. Implications for pathogenesis

The American journal of pathology, 1990-02, Vol.136 (2), p.479-486

1990

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Dendritic cell-lymphoid cell aggregation and major histocompatibility antigen expression during rat cardiac allograft rejection

The Journal of experimental medicine, 1986-10, Vol.164 (4), p.1239-1258

1986

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Role of T helper lymphocytes in autoimmune diseases

Laboratory investigation, 1988-08, Vol.59 (2), p.158

1988

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Hepatitis E virus antibody prevalence

The Lancet (British edition), 1994-10, Vol.344 (8930), p.1166-1166

1994

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SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q

Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutations

Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p

bcl-2 protein expression is associated with better prognosis in colorectal cancer

Expansion of peripheral blood CD5 + B cells is associated with mild disease in chronic hepatitis C virus infection

Post-transplant lymphoproliferative disorder in renal allograft recipients. Clinical experience and risk factor analysis in a single center

Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct

Localization of the Gene for Autosomal Recessive Congenital Hereditary Endothelial Dystrophy (CHED2) to Chromosome 20 by Homozygosity Mapping

Increased major histocompatibility complex antigen expression in unilateral ischemic acute tubular necrosis in the mouse

PROGNOSTIC SIGNIFICANCE OF p53 ABNORMALITIES IN COLORECTAL CARCINOMA DETECTED BY PCR-SSCP AND IMMUNOHISTOCHEMICAL ANALYSIS

Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation

Effects of fenoldopam on renal blood flow and its function in a canine model of rhabdomyolysis

Interferon-gamma gene expression during acute graft-versus-host disease: relationship to MHC induction and tissue injury

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

Effects of fenoldopam on renal blood flow and its function in a canine model of rhabdomyolysis

Squamous cell carcinoma arising in a skin graft donor site following melanoma extirpation at a distant site: A case report and review of the literature

Interferon gamma-mediated renal MHC expression in mercuric chloride-induced glomerulonephritis

Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance

The decreased incidence of aseptic necrosis in renal transplant recipients--a case control study

Cyclosporine-Induced Autoimmunity and Immune Hyperreactivity

In vitro cold activation of complement shown by an overestimation of total complement 4: a study in patients with hepatitis C virus infection

Patterns of MHC antigenic modulation in cyclosporine-induced autoimmunity. Implications for pathogenesis

Dendritic cell-lymphoid cell aggregation and major histocompatibility antigen expression during rat cardiac allograft rejection

Role of T helper lymphocytes in autoimmune diseases

Hepatitis E virus antibody prevalence

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