伴有曲线体的晚发性婴儿神经内脏贮积病 - Suppr

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Late infantile neurovisceral storage disease with curvilinear bodies.

作者信息

Andrews J M, Sorenson V, Cancilla P A, Price H M, Menkes J H

出版信息

Neurology. 1971 Mar;21(3):207-17. doi: 10.1212/wnl.21.3.207.

DOI:10.1212/wnl.21.3.207

PMID:5105407

Abstract

摘要

相似文献

Late infantile neurovisceral storage disease with curvilinear bodies.

Neurology. 1971 Mar;21(3):207-17. doi: 10.1212/wnl.21.3.207.

Juvenile GM2 gangliosidosis. Biochemical and ultrastructural studies on a new variant of Tay-Sachs disease.

Arch Neurol. 1971 Jul;25(1):14-22. doi: 10.1001/archneur.1971.00490010024003.

Gm1-gangliosidosis and juvenile cerebral lipidosis. Clinical, histochemical, and chemical study.

Arch Neurol. 1971 Jun;24(6):529-37. doi: 10.1001/archneur.1971.00480360063008.

[Biochemical study of cerebral and hepatic lipids in a case of Tay-Sachs disease].

Rev Fr Etud Clin Biol. 1969 Jun-Jul;14(6):568-74.

[Generalized GM 1 gangliosidosis: ultrastructure and differential diagnostic importance of storage lymphocytes and bone marrow cells].

Padiatr Padol. 1973;8(3):272-83.

Late infantile systemic lipidosis. Major monosialogangliosidosis. Delineation of two types.

Neurology. 1968 Apr;18(4):340-8. doi: 10.1212/wnl.18.4.340.

A case of GM2-gangliosidosis with total hexosaminidase deficiency.

Neurology. 1970 Apr;20(4):388.

Isolation and chemical characterization of metachromatic granules from a brain with metachromatic leukodystrophy.

J Neuropathol Exp Neurol. 1967 Oct;26(4):537-50. doi: 10.1097/00005072-196710000-00002.

[A disorder of ganglioside metabolism with storage of ceramide lactoside, monosialo ceramide lactoside and Tay-Sachs ganglioside in the brain].

J Neurochem. 1966 Dec;13(12):1273-82. doi: 10.1111/j.1471-4159.1966.tb04290.x.

Juvenile GM 1 gangliosidosis: clinical, pathological, chemical and enzymatic studies.

Clin Genet. 1972;3(6):411-34. doi: 10.1111/j.1399-0004.1972.tb01476.x.

引用本文的文献

[Pigment variant of the adult type of amaurotic idiocy (Kufs) (author's transl)].

Acta Neuropathol. 1973 Nov 5;26(3):225-36. doi: 10.1007/BF00684432.

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

Acta Neuropathol. 1973 Oct 11;26(2):157-70. doi: 10.1007/BF00697751.

Early structural changes in a case of late infantile amaurotic idiocy (early form of Batten-Spielmeyer-Vogt disease).

J Neurol. 1974;207(4):271-8. doi: 10.1007/BF00312581.

Neuronal ceroid-lipofuscin storage in Siamese cats.

Can J Comp Med. 1974 Apr;38(2):207-12.

A case of adult neuronal ceroid-lipofuscinosis with the appearance of membranous cytoplasmic bodies localized in the spinal anterior horn.

Acta Neuropathol. 1987;72(4):362-8. doi: 10.1007/BF00687268.

So-called neuronal ceroid-lipofuscinosis. Histochemical study with evidence of extractibility of the stored material.

Acta Neuropathol. 1977 May 16;38(2):117-22. doi: 10.1007/BF00688557.

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Late infantile neurovisceral storage disease with curvilinear bodies.

作者信息

Andrews J M, Sorenson V, Cancilla P A, Price H M, Menkes J H

出版信息

Neurology. 1971 Mar;21(3):207-17. doi: 10.1212/wnl.21.3.207.

DOI:10.1212/wnl.21.3.207

PMID:5105407

Abstract

摘要

相似文献

Late infantile neurovisceral storage disease with curvilinear bodies.

Neurology. 1971 Mar;21(3):207-17. doi: 10.1212/wnl.21.3.207.

Juvenile GM2 gangliosidosis. Biochemical and ultrastructural studies on a new variant of Tay-Sachs disease.

Arch Neurol. 1971 Jul;25(1):14-22. doi: 10.1001/archneur.1971.00490010024003.

Gm1-gangliosidosis and juvenile cerebral lipidosis. Clinical, histochemical, and chemical study.

Arch Neurol. 1971 Jun;24(6):529-37. doi: 10.1001/archneur.1971.00480360063008.

[Biochemical study of cerebral and hepatic lipids in a case of Tay-Sachs disease].

Rev Fr Etud Clin Biol. 1969 Jun-Jul;14(6):568-74.

[Generalized GM 1 gangliosidosis: ultrastructure and differential diagnostic importance of storage lymphocytes and bone marrow cells].

Padiatr Padol. 1973;8(3):272-83.

Late infantile systemic lipidosis. Major monosialogangliosidosis. Delineation of two types.

Neurology. 1968 Apr;18(4):340-8. doi: 10.1212/wnl.18.4.340.

A case of GM2-gangliosidosis with total hexosaminidase deficiency.

Neurology. 1970 Apr;20(4):388.

Isolation and chemical characterization of metachromatic granules from a brain with metachromatic leukodystrophy.

J Neuropathol Exp Neurol. 1967 Oct;26(4):537-50. doi: 10.1097/00005072-196710000-00002.

[A disorder of ganglioside metabolism with storage of ceramide lactoside, monosialo ceramide lactoside and Tay-Sachs ganglioside in the brain].

J Neurochem. 1966 Dec;13(12):1273-82. doi: 10.1111/j.1471-4159.1966.tb04290.x.

Juvenile GM 1 gangliosidosis: clinical, pathological, chemical and enzymatic studies.

Clin Genet. 1972;3(6):411-34. doi: 10.1111/j.1399-0004.1972.tb01476.x.

引用本文的文献

[Pigment variant of the adult type of amaurotic idiocy (Kufs) (author's transl)].

Acta Neuropathol. 1973 Nov 5;26(3):225-36. doi: 10.1007/BF00684432.

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

Acta Neuropathol. 1973 Oct 11;26(2):157-70. doi: 10.1007/BF00697751.

Early structural changes in a case of late infantile amaurotic idiocy (early form of Batten-Spielmeyer-Vogt disease).

J Neurol. 1974;207(4):271-8. doi: 10.1007/BF00312581.

Neuronal ceroid-lipofuscin storage in Siamese cats.

Can J Comp Med. 1974 Apr;38(2):207-12.

A case of adult neuronal ceroid-lipofuscinosis with the appearance of membranous cytoplasmic bodies localized in the spinal anterior horn.

Acta Neuropathol. 1987;72(4):362-8. doi: 10.1007/BF00687268.

So-called neuronal ceroid-lipofuscinosis. Histochemical study with evidence of extractibility of the stored material.

Acta Neuropathol. 1977 May 16;38(2):117-22. doi: 10.1007/BF00688557.