Infantile osteopetrosis complicating neuronal ceroid lipofuscinosis (Q48852679)

16 February 2018

title

Infantile osteopetrosis complicating neuronal ceroid lipofuscinosis (English)

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16 February 2018

author name string

Takahashi K

1

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16 February 2018

Naito M

2

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16 February 2018

Yamamura F

3

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16 February 2018

Taki T

4

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16 February 2018

Sugino S

5

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16 February 2018

Taku K

6

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16 February 2018

Miike T

7

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16 February 2018

publication date

1 December 1990

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16 February 2018

Pathology, Research and Practice

published in

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16 February 2018

volume

186

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16 February 2018

issue

6

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16 February 2018

page(s)

697-706

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16 February 2018

Infantile osteopetrosis and neuronal storage disease

cites work

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An ultramicroscopic study of the skin in the diagnosis of the infantile and late infantile types of ceroid-lipofuscinosis

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A dominant form of neuronal ceroid-lipofuscinosis. An ultrastructural study of sural nerve and peripheral lymphocytes.

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Infantile Form of So-Called Neuronal Ceroid Lipofuscinosis: Lipid Biochemical Studies, Fatty Acid Analysis of Cerebroside Sulfatides and Sphingomyelin, Myelin Density Profile and Lipid Composition

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Studies on osteopetrosis. III. Roentgenological and pathologic-anatomical investigations on some of the bone changes

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Ultrastructural investigations of peripheral nerves in neuronal ceroid-lipofuscinoses (NCL).

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7 January 2021

Polyunsaturated fatty acid lipidosis infantile form of so-called neuronal ceroidlipofuscinosis

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7 January 2021

Infantile type of so-called neuronal ceroid-lipofuscinosis. Histological and electron microscopic studies

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Infantile type of so-called neuronal ceroid-lipofuscinosis. 2. Morphological and biochemical studies

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Neurological complications of infantile osteopetrosis

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7 January 2021

Clinical and extraneural histologic diagnosis of neuronal ceroid-lipofuscinosis

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Cytoplasmic inclusions in the vermiform appendix and skeletal muscle in two types of so-called neuronal ceroid-lipofuscinosis

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7 January 2021

Suction biopsy of rectal mucosa in the diagnosis of infantile and juvenile types of neuronal ceroid lipofuscinoses

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The pathogenesis of infantile malignant osteopetrosis: Bone mineral metabolism and complications in five infants

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Monoclonal antibody defining a stage-specific mouse embryonic antigen (SSEA-1)

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Large alterations in ganglioside and neutral glycosphingolipid patterns in brains from cases with infantile neuronal ceroid lipofuscinosis/polyunsaturated fatty acid lipidosis

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Glycolipids of metastatic tissue in liver from colon cancer: appearance of sialylated Le(x) and Le(x) lipids

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Malignant osteopetrosis: a disease of abnormal osteoclast osteoclast proliferation

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Osteoclast abnormalities in idiopathic osteopetrosis. Reference to the ultrastructural histochemistry study

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7 January 2021

Clinico-pathological variability in the childhood neuronal ceroid-lipofuscinoses and new observations on glycoprotein abnormalities

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7 January 2021

Diagnosis of late infantile neuronal “ceroid-lipofuscinosis” from histochemical and ultrastructural changes in dental pulp

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7 January 2021

Developmental changes in ganglioside composition and synthesis in embryonic rat brain.

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7 January 2021

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Identifiers

DOI

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1 reference

16 February 2018