Enzyme replacement therapy by renal allotransplantation in Fabry's disease.

No abstract is available for this paper.

• Publication year

  1972

• Venue

  New England Journal of Medicine

• Publication date

  1972-12-14

• Fields of study

  Medicine

• Identifiers
  DOI 10.1056/NEJM197212142872402PMID 4563677
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Quantitative analysis of phospholipids by thin-layer chromatography and phosphorus analysis of spots

  2007cited by this paper
• Biochemical Studies on GM1-Gangliosidosis and Ceramide Trihexosidosis

  1972cited by this paper
• Studies on the Metabolic Control of Fabry’s Disease Through Kidney Transplantation

  1972cited by this paper
• Chemistry and Metabolism of Glycosphingolipids in Fabry’s Disease

  1972cited by this paper
• Reversal of an inborn sphingolipidosis (Fabry's disease) by kidney transplantation.

  1972cited by this paper
• the central nervous system in Fabry's disease. A clinical, pathological, and biochemical investigation.

  1971cited by this paper
• Evidence for a terminal -D-galactopyranosyl residue in galactosylgalactosylglucosylceramide from human kidney.

  1971cited by this paper
• Neutral glycolipids in leukemic and nonleukemic leukocytes.

  1971cited by this paper
• Treatment of Fabry's disease: correction of the enzymatic deficiency by renal transplantation.

  1971cited by this paper
• Further observations on the role of the adenyl cyclase-cyclic AMP (CAMP) system in human lipolysis.

  1971cited by this paper
• Ceramide trihexosidosis (fabry's disease) without skin lesions.

  1971cited by this paper
• Enzyme Replacement in Fabry's Disease, an Inborn Error of Metabolism

  1970cited by this paper
• In vivo studies on glycosphingolipid metabolism in porcine blood.

  1970cited by this paper
• Galactosylgalactosylglucosylceramide: Galactosyl hydrolase in normal human plasma and its absence in patients with fabry's disease

  1970cited by this paper
• A method for the quantitative determination of neutral glycosphingolipids in urine sediment.

  1970cited by this paper
• Concentrations of glycosyl ceramides in plasma and red cells in Fabry's disease, a glycolipid lipidosis.

  1969cited by this paper
• Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency.

  1967cited by this paper
• [Angiokeratoma corporis diffusum (Fabry's disease)].

  1967cited by this paper
• Quantitative determination of the neutral glycosyl ceramides in human blood.

  1967cited by this paper
• Neutral glycolipids of human kidney isolation, identification, and fatty acid composition.

  1966cited by this paper
• Quantitative estimation of sialic acids. II. A colorimetric resorcinol-hydrochloric acid method.

  1957cited by this paper
• A simple method for the isolation and purification of total lipides from animal tissues.

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• THE QUANTITATIVE ESTIMATION OF CEREBROSIDES IN NERVOUS TISSUE

  1956cited by this paper
• Angiokeratoma corporis diffusum (universale) Fabry, as a sign of an unknown internal disease; two autopsy reports.

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• Outcomes and management of kidney transplant recipients with Fabry disease: a review

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• Outcomes of Kidney Transplantation in Fabry Disease: A Meta-Analysis

  2020cites this paper
• Kidney Transplant in Fabry Disease: A Revision of the Literature

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• Long-term Outcomes of Kidney Transplantation in Fabry Disease

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• Early markers of heart and kidney damage in Fabry disease

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• Low frequency of Fabry disease in patients with common heart disease

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• Prenatal Diagnosis of Disorders of Lipid Metabolism

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• The kidney in Fabry's disease

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• Risk of Death in Heart Disease is Associated With Elevated Urinary Globotriaosylceramide

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• Fabry Disease (α-Galactosidase A Deficiency)

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• Genetic Abnormalities in Glomerular Function

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• Biomarkers of Fabry disease nephropathy.

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• Therapeutic Implications of Renal Transplantation in a Patient with Fabry's Disease

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• Clinical and diagnostic considerations in Fabry's disease.

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• Fabry Disease (α-Galactosidase A Deficiency): An X-linked Nephropathy

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• [Kidney transplantation in Fabry disease].

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• CHAPTER 85 – Genetic Abnormalities in Glomerular Function

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• Agalsidase therapy in patients with Fabry disease on renal replacement therapy: a nationwide study in Italy.

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• Pseudo-developmental glaucoma

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• Nephrology Dialysis Transplantation Recurrence of Fabry ' s disease in a renal allograft 14 years after transplantation

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• Enzyme replacement therapy of fabry disease

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• Fabry disease in the era of enzyme replacement therapy: a renal perspective

  2004cites this paper
• Enzyme replacement therapy for Fabry disease, an inherited nephropathy.

  2002cites this paper
• Natural History of Fabry Renal Disease: Influence of α-Galactosidase A Activity and Genetic Mutations on Clinical Course

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• Fabry disease (alpha-galactosidase A deficiency): renal involvement and enzyme replacement therapy.

  2001cites this paper
• Fabry Disease (α-Galactosidase A Deficiency): Renal Involvement and Enzyme Replacement Therapy

  2001cites this paper
• Das Herz bei Stoffwechselerkrankungen

  2000cites this paper
• Enzymatic corrections for cells derived from Fabry disease patients by a recombinant adenovirus vector

  2000cites this paper
• Infusion of α-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease

  2000cites this paper
• Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease.

  2000cites this paper
• A case of Fabry's disease with normal kidney function at 10 years after successful renal transplantation.

  1998cites this paper
• Renal transplantation in patients with hereditary kidney disease: our experience.

  1997cites this paper
• Manifestations ostéoarticulaires des maladies de surcharge (III)

  1996cites this paper
• Novel frameshift mutation in a heterozygous woman with Fabry disease and end-stage renal failure.

  1996cites this paper
• Report on management of renale failure in Europe, XXVI, 1995. Rare diseases in renal replacement therapy in the ERA-EDTA Registry.

  1996influential citation
• Recurrence of Fabry's disease in a renal allograft eleven years after successful renal transplantation.

  1991cites this paper
• Enteric spherules diastase in enzyme preparations.

  1991cites this paper
• Recurrent disease after renal transplantation

  1991cites this paper
• Fabry’s disease: A family study

  1990cites this paper
• Recurrence of disease following renal transplantation.

  1988cites this paper
• [Diagnosis of Fabry's disease].

  1987cites this paper
• Renal biopsy in Fabry's disease eight years after successful renal transplantation.

  1987cites this paper
• Natural history and treatment of uremia secondary to Fabry's disease: an European experience.

  1987cites this paper
• Involvement of renal allograft by Fabry's disease.

  1987cites this paper
• Disorders of Lipid Metabolism

  1986cites this paper
• Immune function and renal transplantation in Fabry's disease.

  1985cites this paper
• ENZYME REPLACEMENT IN THE SPHINGOLIPIDOSES

  1984cites this paper
• TRANSPLANTATION IN RELATION TO THE TREATMENT OF INHERITED DISEASE

  1984cites this paper
• Ultrastructural changes in the cornea and conjunctiva of a heterozygous woman with Fabry's disease.

  1984cites this paper
• Fabry's disease. An X-linked inherited metabolic disorder.

  1984cites this paper
• [Fabry's disease. Light and electron microscopic cardiac findings 12 years after successful kidney transplantation].

  1982cites this paper
• Renal Transplantation in Anderson-Fabry Disease

  1982cites this paper
• Anderson--Fabry disease.

  1982cites this paper
• Enzyme substitution by fibroblast transplantation

  1982cites this paper
• Prospects for enzyme replacement therapy in heritable metabolic disorders

  1982cites this paper
• Advances in the treatment of inherited metabolic diseases.

  1981cites this paper
• Ten-year experience in renal transplantation for Fabry's disease.

  1981cites this paper
• [Neuropathy associated with ichthyosis and splenomegaly in an adult patient. Possible relationship with altered glycosphingolipid metabolism (author's transl)].

  1981cites this paper
• Correction of Lysosomal Enzyme Deficiences by Enzyme Replacement

  1981cites this paper
• Light- and electron-microscopic histochemistry of Fabry's disease.

  1981cites this paper
• Plasma exchange removes glycosphingolipid in Fabry disease.

  1980cites this paper
• Proceedings of the Annual Meeting of the European Foundation for Bone Marrow Transplantation, Sils Maria (Engadine), Switzerland, April 13-16, 1980.

  1980cites this paper
• Proceedings of the Annual Meeting of the European Foundation for Bone Marrow Transplantation

  1980cites this paper
• The Biochemical Basis of Disease

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• Attempt at enzyme replacement by fetal liver transplantation in Fabry's disease.

  1979cites this paper
• [Fabry's disease: two patients improved by fetal liver cells (author's transl)].

  1979cites this paper
• Uses and abuses of chlormethiazole.

  1979cites this paper
• Uses and abuses of chlormethiazole.

  1979cites this paper
• Renal transplantation (first of two parts).

  1979cites this paper
• Prenatal Diagnosis of Hereditary Biochemical Disorders of Metabolism

  1979cites this paper
• [Clinical, preclinical and prenatal diagnosis of congenital sphingolipidoses by determining lysosomal hydrolases (author's transl)].

  1978cites this paper
• Clinical and experimental transplantation in enzymatic deficiency disease.

  1978cites this paper
• 5 – Glycolipid Catabolism

  1978cites this paper
• Eye findings in the diagnosis of Fabry's disease. Patients with renal failure.

  1978cites this paper
• Sphingolipidoses.

  1978cites this paper
• Early renal changes in hemizygous and heterozygous patients with Fabry's disease.

  1978cites this paper
• Angiokeratoma corporis diffusum: the evolution of a disease entity.

  1977cites this paper
• The surgeon, genetics, and cancer control: the Cancer Family Syndrome.

  1977cites this paper
• Delayed diagnosis in angiokeratoma corporis diffusum (Anderson-Fabry's disease).

  1977cites this paper
• Replacement therapy for inherited enzyme deficiency: liver orthotopic transplantation in Niemann-Pick disease type A.

  1977cites this paper
• A Biomedical View of Enzyme Replacement Strategies in Genetic Disease

  1977cites this paper
• Progressive muscular dystrophy. Functional improvement after a renal allograft.

  1976cites this paper
• [Fabry's disease (angiokeratoma corporis diffusum universale): benign course after kidney transplantation].

  1976cites this paper
• B.C.P. Jansen Institute, University of Amsterdam, Amsterdam, The Netherlands.

  1976cites this paper
• Neutral glycosphingolipids of serum lipoproteins in Fabry's disease.

  1976cites this paper
• Fabry’s Disease—Angiokeratoma Corporis Diffusum Universale

  1976cites this paper
• Study on a family with anderson--Fabry's disease and associated familial spastic paraplegia.

  1976cites this paper
• Failure to correct the metabolic defect by renal allotransplantion in Fabry's disease.

  1976cites this paper
• [Renal transplantation in patients suffering from Fabry's disease. Kidney transplantation from an heterozygote subject to a subject without Fabry's disease].

  1975cites this paper
• [Differential diagnosis of congenital lipidoses by lipid analyses of body fluids, biopsy and autopsy tissue].

  1975cites this paper
• The treatment of genetic disorders.

  1975cites this paper
• Hereditary disease and its control.

  1975cites this paper
• [Fabry's diffuse angiokeratoma corporis].

  1975cites this paper
• Inherited disorders of lysosomal metabolism.

  1975cites this paper
• Cardiac manifestations of Fabry's disease. Report of a case with mitral insufficiency and electrocardiographic evidence of myocardial infarction.

  1975cites this paper
• ステロイドが著効を呈したFabry病(angiokeratoma corporis diffusum)の初期の1例

  1975cites this paper
• Das Angiokeratoma corporis diffusum Fabry

  1975cites this paper
• Gel entrapment of enzyme. A strategy for enzyme correction.

  1974cites this paper
• An enzymological approach to the lipidoses.

  1974cites this paper
• Present status of kidney transplantation.

  1974cites this paper