LIPOID PROTEINOSIS. I: THE CLINICAL PICTURE.
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Adolescent↗
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Results for “LIPOIDOSIS”
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[THE HISTOCHEMICAL DEMONSTRATION OF MUCOPOLYSACCHARIDES IN SULFATIDE GRANULES DURING THE INTRACELLULAR STORAGE OF CEREBROSIDE SULFATE ESTERS].
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Brain Chemistry↗
AMAUROTIC IDIOCY AND EPILEPSY.
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Diagnosis↗
A case of the Hand-Schüller-Christian disease treated with cortisone; a discussion of the primary or secondary nature of the lipoid deposits.
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Cortisone↗
Another case of Niemann-Pick's disease observed in Denmark.
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Denmark↗
[The identity of the Tay-Sachs and Niemann-Pick diseases].
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Intellectual Disability↗
THE EXCRETION OF URINARY SULFATIDES IN HEALTH AND NEUROLOGICAL DISEASE.
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Adolescent↗
DIETARY treatment of essential familial xanthomatosis.
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Diet↗
SERUM lipids and xanthomatous disease.
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Blood↗
CHOLESTEROL CONTENT OF RABBIT AORTA AFTER CESSATION OF CHOLESTEROL FEEDING.
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Animals↗
MUTANT MICE (QUAKING AND JIMPY) WITH DEFICIENT MYELINATION IN THE CENTRAL NERVOUS SYSTEM.
Two mutant mice with deficient myelination are described. Quaking is a new autosomal recessive mutant mouse with marked tremor of the hindquarters. The mice eat, swim, breed, and nurse well even though the entire central nervous system is very deficient in myelin by histological and chemical criteria. Myelin formation is impaired; no destruction is seen. Peripheral nerves are myelinated. Jimpy, a known sex-linked mutation, has similar but more severe symptoms and similar pathology, with the additional feature of sudanophilic (nonpolar) lipid distributed in some white-matter tracts. Both mutants offer new opportunities for study of the formation and functions of myelin.
Animals↗
Honeycomb lung and xanthomatosis.
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Humans↗
Rare features in a case of Gaucher's disease.
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Gaucher Disease↗
LIPIDPROTEINOSIS (URBACH-WIETHE SYNDROME).
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Adolescent↗
RETINAL NEUROPATHOLOGY OF LATE INFANTILE AMAUROTIC IDIOCY.
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Child↗
Pregnancy and Gaucher's disease.
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Female↗