HURLER'S SYNDROME: A HISTOCHEMICAL STUDY. NEW TECHNIQUES FOR LOCALIZATION OF VERY WATER-SOLUBLE ACID MUGOPOLYSACCHARIDES.

No abstract is available for this paper.

• Publication year

  1964

• Venue

  American Journal of Pathology

• Publication date

  1964-12-01

• Fields of study

  Medicine

• Identifiers
  PMID 14241525PMCID PMC1907165
• 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.

• THE VISCERAL LESIONS OF METACHROMATIC LEUKODYSTROPHY.

  1964cited by this paper
• The production of sulphated mucopolysaccharides by endothelium.

  1962cited by this paper
• Histochemical and electron microscopic study in a case of Hurler's disease.

  1962cited by this paper
• Hurler's syndrome.

  1961cited by this paper
• HISTOCHEMICAL STUDIES IN HURLER'S DISEASE: A NEW METHOD FOR LOCALIZATION OF ACID MUCOPOLYSACCHARIDE, AND AN ANALYSIS OF LEAD ACETATE "FIXATION"

  1961cited by this paper
• Excretion of Sulfated Mucopolysaccharides in Gargoylism. (Hurler's Syndrome)∗

  1958cited by this paper
• Chemical nature of the storage substance in gargoylism, Hurler-Pfaundler's disease.

  1955cited by this paper
• The histology and histochemistry of gargoylism.

  1954cited by this paper
• Gargoylism; a mucopolysaccharidosis.

  1952cited by this paper
• Gargoylism; study of pathologic lesions and clinical review of 12 cases.

  1948cited by this paper

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  2020cites this paper
• Developmental and Inherited Liver Disease

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• Decreased performance in IDUA knockout mouse mimic limitations of joint function and locomotion in patients with Hurler syndrome

  2015cites this paper
• The Pathology of the Skeleton in Lysosomal Storage Diseases

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• mucopolysaccharidosis. MR imaging of the brain in patients with

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• 4 – Genetic and metabolic liver disease

  2012cites this paper
• The contribution of chemical exchange to MRI frequency shifts in brain tissue

  2011cites this paper
• Cerebral infarction in Hunter syndrome.

  2006cites this paper
• Keratopathy in rats after treatment with tilorone

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• Stoffwechselerkrankungen der Leber

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• Sulfamidase Deficiency in a Family of Dachshunds: A Canine Model of Mucopolysaccharidosis IIIA (Sanfilippo A)

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• Severe type Hunter's syndrome. Polysomnographic and neuropathological study.

  1992cites this paper
• MR imaging of the brain in patients with mucopolysaccharidosis.

  1989cites this paper
• HUNTER'S SYNDROME. An Ultrastructural Study of an Autopsy Case

  1988cites this paper
• Mucopolysaccharidosis-like alterations in cardiac valves of rats treated with tilorone

  1985cites this paper
• Histochemical demonstration of cytoplasmic glycosaminoglycans in the macroneurons of the human central nervous system

  1984cites this paper
• The Pathology of the Spine

  1980cites this paper
• Prenatal Mucopolysaccharidosis II (Hunter): A Pathogenetic Study

  1980cites this paper
• Morphological observations in the nervous system of prenatal mucopolysaccharidosis II (M. Hunter)

  1979cites this paper
• Sanfilippo A syndrome in the fetus

  1978cites this paper
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  1977cites this paper
• Mucopolysaccharidosis types I, II, IIIA and V

  1977cites this paper
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  1977cites this paper
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  1976cites this paper
• Mucopolysaccharidosis type V. (Scheie syndrome). A postmortem study by multidisciplinary techniques with emphasis on the brain.

  1976cites this paper
• The heart in the Hurler syndrome: gross, histologic and ultrastructural observations in five necropsy cases.

  1976cites this paper
• MORPHOLOGICAL AND BIOCHEMICAL STUDIES OF A CASE OF MUCOPOLYSACCHARIDOSIS II (HUNTER'S SYNDROME)

  1976cites this paper
• [Study of leukocyte gangliosides in various types of mucopolysaccharidosis].

  1975cites this paper
• Diseases of Carbohydrate Metabolism

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• Mucopolysaccharidoses and mucolipidoses

  1974cites this paper
• Pituitary gland in patients with Hurler syndrome. Light and electron microscopic study.

  1974cites this paper
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  1973cites this paper
• [Mucopolysaccharidosis of the Pfaundler-Hurler type with spastic tetraparesis and retinitis pigmentosa of two adult sisters].

  1972cites this paper
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  1972cites this paper
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  1972cites this paper
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  1972cites this paper
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  1971cites this paper
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  1971cites this paper
• MUCOPOLYSACCHARIDOSIS TYPE III (SANFILIPPO'S SYNDROME)

  1971cites this paper
• [Ultrastructural study of the hepatic parenchyma in mucopolysaccharidosis].

  1970cites this paper
• Hyaluronidase and sulfatase deficiency in Hurler's syndrome.

  1970cites this paper
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  1970cites this paper
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  1969cites this paper
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  1969cites this paper
• The nosology of the mucopolysaccharidoses.

  1969cites this paper
• [Ultrastructural study of the liver in Morquio's disease].

  1969cites this paper
• CLINICAL, BIOCHEMICAL AND ULTRASTRUCTURAL STUDIES OF AN ATYPICAL FORM OF MUCOPOLYSACCHARIDOSIS

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  1968cites this paper
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  1968cites this paper
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  1968cites this paper
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  1967cites this paper
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• STUDIES ON THE GENETICS OF THE HURLER–HUNTER SYNDROME*

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• [HS-mucopolysaccharidosis of Sanfilippo (polydystrophic oligophrenia). A report on 10 patients].

  1967cites this paper
• [Farber's disease (disseminated lipogranulomatosis). Clinical picture and summary of the chemical findings].

  1967cites this paper
• [The heparitinsulfate mucopolysaccharidosis (Sanfilippo). Clinical, biochemical, genetic and morphological studies].

  1967cites this paper
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• Mucopolysaccharides of whole human spleens in generalized amyloidosis.

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• Mental Subnormality in Hunter‐Hurler Syndrome (Gargoylism): A Suggested Biochemical Cause

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• Mucopolysaccharidosis type 3. Morphologic and biochemical studies of two siblings with Sanfilippo syndrome.

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