黏多糖贮积症Ⅱ型患者两份脑活检组织的电子显微镜检查 - Suppr

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ELECTRON MICROSCOPY OF TWO CEREBRAL BIOPSIES IN GARGOYLISM.

作者信息

ALEU F P, TERRY R D, ZELLWEGER H

出版信息

J Neuropathol Exp Neurol. 1965 Apr;24:304-17. doi: 10.1097/00005072-196504000-00010.

DOI:10.1097/00005072-196504000-00010

PMID:14280504

Abstract

摘要

相似文献

ELECTRON MICROSCOPY OF TWO CEREBRAL BIOPSIES IN GARGOYLISM.

J Neuropathol Exp Neurol. 1965 Apr;24:304-17. doi: 10.1097/00005072-196504000-00010.

ULTRASTRUCTURAL AND BIOCHEMICAL OBSERVATIONS ON A CASE OF SYSTEMIC LATE INFANTILE LIPIDOSIS AND ITS RELATIONSHIP TO TAY-SACHS DISEASE AND GARGOYLISM.

J Neuropathol Exp Neurol. 1965 Apr;24:318-40. doi: 10.1097/00005072-196504000-00011.

STRUCTURE COMPARISON OF THE MAJOR MONOSIALOGANGLIOSIDES FROM BRAINS OF NORMAL HUMAN, GARGOYLISM, AND LATE INFANTILE SYSTEMIC LIPIDOSIS. I.

J Neuropathol Exp Neurol. 1965 Apr;24:341-51. doi: 10.1097/00005072-196504000-00012.

FORMATION OF THE MEMBRANOUS CYTOPLASMIC BODIES IN TAY-SACHS DISEASE: AN IN VITRO STUDY.

J Neuropathol Exp Neurol. 1965 Apr;24:256-64. doi: 10.1097/00005072-196504000-00007.

[ULTRASTRUCTURE OF THE HEPATIC CELLS IN HURLER'S DISEASE (GARGOYLISM)].

C R Hebd Seances Acad Sci. 1964 Aug 3;259:1281-3.

TAY-SACHS DISEASE WITH VISCERAL INVOLVEMENT AND ITS RELATION TO GARGOYLISM.

Arch Dis Child. 1964 Dec;39(208):634-40. doi: 10.1136/adc.39.208.634.

STAINING OF ISOLATED ABNORMAL NEURONAL CYTOSOMES.

Stain Technol. 1964 Jul;39:215-7. doi: 10.3109/10520296409061232.

LATE INFANTILE AMAUROTIC IDIOCY. ULTRAMICROSCOPIC AND HISTOCHEMICAL STUDIES ON A CASE.

Arch Pathol. 1964 Nov;78:483-500.

G5-ganglioside variant of systemic late infantile lipidosis. Generalized gangliosidosis.

Arch Pathol. 1969 Apr;87(4):393-403.

Hurler's and Sanfilippo's variants of mucopolysaccharidosis. Cerebral pathology and lipid chemistry.

Arch Pathol. 1971 May;91(5):434-43.

引用本文的文献

Mutations in vacuolar H+ -ATPase subunits lead to biliary developmental defects in zebrafish.

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J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S67-72. doi: 10.1007/s10545-009-9023-8. Epub 2010 Jan 6.

Lysosomal accumulation of SCMAS (subunit c of mitochondrial ATP synthase) in neurons of the mouse model of mucopolysaccharidosis III B.

Mol Genet Metab. 2007 Apr;90(4):393-401. doi: 10.1016/j.ymgme.2006.11.006. Epub 2006 Dec 20.

Ultrastructure of myocardium in the Hurler syndrome. Possible relation to cardiac function.

Virchows Arch A Pathol Anat Histol. 1982;394(3):195-205. doi: 10.1007/BF00430665.

Morphological study on the hereditary neurogenic amyotrophic dogs: accumulation of lipid compound-like structures in the lower motor neuron.

Acta Neuropathol. 1983;61(3-4):270-4. doi: 10.1007/BF00691997.

The AB-variant of GM2-gangliosidosis. Clinical, biochemical, and pathological studies of two patients.

Acta Neuropathol. 1980;52(3):189-202. doi: 10.1007/BF00705807.

[Amaurotic idiocy connected with metachromatic leukodystrophy: transitional form or combination? Electron microscopic and histochemical finding].

Acta Neuropathol. 1967 May 5;8(3):292-308. doi: 10.1007/BF00688830.

Accumulation of smooth cisterns, multivesicular bodies and "zebra" bodies in neurons. A case of peculiar storage condition.

Acta Neuropathol. 1971;18(2):132-43. doi: 10.1007/BF00687601.

[The ultrastructure of protagon (pi) granules].

Acta Neuropathol. 1970;15(1):56-69. doi: 10.1007/BF00690689.

[Neuro-muscular biopsy in the diagnosis of infantile neuroaxonal dystrophy. Ultrastructural study of 3 cases 2 of them familial].

Acta Neuropathol. 1972;21(2):109-16. doi: 10.1007/BF00687565.

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ELECTRON MICROSCOPY OF TWO CEREBRAL BIOPSIES IN GARGOYLISM.

作者信息

ALEU F P, TERRY R D, ZELLWEGER H

出版信息

J Neuropathol Exp Neurol. 1965 Apr;24:304-17. doi: 10.1097/00005072-196504000-00010.

DOI:10.1097/00005072-196504000-00010

PMID:14280504

Abstract

摘要

相似文献

ELECTRON MICROSCOPY OF TWO CEREBRAL BIOPSIES IN GARGOYLISM.

J Neuropathol Exp Neurol. 1965 Apr;24:304-17. doi: 10.1097/00005072-196504000-00010.

ULTRASTRUCTURAL AND BIOCHEMICAL OBSERVATIONS ON A CASE OF SYSTEMIC LATE INFANTILE LIPIDOSIS AND ITS RELATIONSHIP TO TAY-SACHS DISEASE AND GARGOYLISM.

J Neuropathol Exp Neurol. 1965 Apr;24:318-40. doi: 10.1097/00005072-196504000-00011.

STRUCTURE COMPARISON OF THE MAJOR MONOSIALOGANGLIOSIDES FROM BRAINS OF NORMAL HUMAN, GARGOYLISM, AND LATE INFANTILE SYSTEMIC LIPIDOSIS. I.

J Neuropathol Exp Neurol. 1965 Apr;24:341-51. doi: 10.1097/00005072-196504000-00012.

FORMATION OF THE MEMBRANOUS CYTOPLASMIC BODIES IN TAY-SACHS DISEASE: AN IN VITRO STUDY.

J Neuropathol Exp Neurol. 1965 Apr;24:256-64. doi: 10.1097/00005072-196504000-00007.

[ULTRASTRUCTURE OF THE HEPATIC CELLS IN HURLER'S DISEASE (GARGOYLISM)].

C R Hebd Seances Acad Sci. 1964 Aug 3;259:1281-3.

TAY-SACHS DISEASE WITH VISCERAL INVOLVEMENT AND ITS RELATION TO GARGOYLISM.

Arch Dis Child. 1964 Dec;39(208):634-40. doi: 10.1136/adc.39.208.634.

STAINING OF ISOLATED ABNORMAL NEURONAL CYTOSOMES.

Stain Technol. 1964 Jul;39:215-7. doi: 10.3109/10520296409061232.

LATE INFANTILE AMAUROTIC IDIOCY. ULTRAMICROSCOPIC AND HISTOCHEMICAL STUDIES ON A CASE.

Arch Pathol. 1964 Nov;78:483-500.

G5-ganglioside variant of systemic late infantile lipidosis. Generalized gangliosidosis.

Arch Pathol. 1969 Apr;87(4):393-403.

Hurler's and Sanfilippo's variants of mucopolysaccharidosis. Cerebral pathology and lipid chemistry.

Arch Pathol. 1971 May;91(5):434-43.

引用本文的文献

Mutations in vacuolar H+ -ATPase subunits lead to biliary developmental defects in zebrafish.

Dev Biol. 2012 May 15;365(2):434-44. doi: 10.1016/j.ydbio.2012.03.009. Epub 2012 Mar 16.

Hunter syndrome in an 11-year old girl on enzyme replacement therapy with idursulfase: brain magnetic resonance imaging features and evolution.

J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S67-72. doi: 10.1007/s10545-009-9023-8. Epub 2010 Jan 6.

Lysosomal accumulation of SCMAS (subunit c of mitochondrial ATP synthase) in neurons of the mouse model of mucopolysaccharidosis III B.

Mol Genet Metab. 2007 Apr;90(4):393-401. doi: 10.1016/j.ymgme.2006.11.006. Epub 2006 Dec 20.

Ultrastructure of myocardium in the Hurler syndrome. Possible relation to cardiac function.

Virchows Arch A Pathol Anat Histol. 1982;394(3):195-205. doi: 10.1007/BF00430665.

Morphological study on the hereditary neurogenic amyotrophic dogs: accumulation of lipid compound-like structures in the lower motor neuron.

Acta Neuropathol. 1983;61(3-4):270-4. doi: 10.1007/BF00691997.

The AB-variant of GM2-gangliosidosis. Clinical, biochemical, and pathological studies of two patients.

Acta Neuropathol. 1980;52(3):189-202. doi: 10.1007/BF00705807.

[Amaurotic idiocy connected with metachromatic leukodystrophy: transitional form or combination? Electron microscopic and histochemical finding].

Acta Neuropathol. 1967 May 5;8(3):292-308. doi: 10.1007/BF00688830.

Accumulation of smooth cisterns, multivesicular bodies and "zebra" bodies in neurons. A case of peculiar storage condition.

Acta Neuropathol. 1971;18(2):132-43. doi: 10.1007/BF00687601.

[The ultrastructure of protagon (pi) granules].

Acta Neuropathol. 1970;15(1):56-69. doi: 10.1007/BF00690689.

[Neuro-muscular biopsy in the diagnosis of infantile neuroaxonal dystrophy. Ultrastructural study of 3 cases 2 of them familial].

Acta Neuropathol. 1972;21(2):109-16. doi: 10.1007/BF00687565.