[假肌病性脊髓性肌萎缩症（沃尔夫哈特-库格尔伯格-韦兰德型）肌肉变化的组织学-组织化学研究] - Suppr

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超能文献

[Histological-histochemical studies on muscular changes in pseudomyopathic spinal muscular atrophy (Wohlfart-Kugelberg-Welander)].

作者信息

Heene R

出版信息

Z Neurol. 1970;198(3):291-304.

PMID:4102127

Abstract

摘要

相似文献

[Histological-histochemical studies on muscular changes in pseudomyopathic spinal muscular atrophy (Wohlfart-Kugelberg-Welander)].[假肌病性脊髓性肌萎缩症（沃尔夫哈特-库格尔伯格-韦兰德型）肌肉变化的组织学-组织化学研究]

Z Neurol. 1970;198(3):291-304.

Ultrastructural and histochemical features of skeletal muscle in the Wohlfart-Kugelberg-Welander syndrome.沃夫哈特-库格尔伯格-韦兰德综合征中骨骼肌的超微结构和组织化学特征。

J Neurol Sci. 1971 May;13(1):13-25. doi: 10.1016/0022-510x(71)90204-8.

[Case of apparently primary lactic acidosis in a subject with Kugelberg-Welander pseudomyopathic muscular atrophy].[库格尔贝格-韦兰德假性肌病性肌肉萎缩患者原发性乳酸酸中毒病例]

Minerva Med. 1970 Dec 8;61(98):5677-83.

Juvenile spinal muscular atrophy (Wohlfart Kugelberg Welander Disease): a case report.青少年型脊髓性肌萎缩症（沃夫哈特-库格伯格-韦兰德病）：一例病例报告。

Indian Pediatr. 1976 May;13(5):387-8.

Werdnig-Hoffmann-Wohlfart-Kugelberg-Welander disease. Nosological unity and clinical variability in intrafamilial cases.韦尔尼格－霍夫曼－沃尔夫法特－库格尔贝格－韦兰德病。家族性病例中的疾病分类一致性与临床变异性。

Acta Genet Med Gemellol (Roma). 1971 Jan;20(1):43-58. doi: 10.1017/s1120962300011707.

[Pseudomyopathic spinal muscular atrophy (type Kugelberg-Welander) with malformed limbs (author's transl)].伴有肢体畸形的假肌病性脊髓性肌萎缩（库格尔贝格－韦兰德型）（作者译）

Dtsch Med Wochenschr. 1974 Nov 22;99(47):2400, 3-4. doi: 10.1055/s-0028-1108146.

[A case of Wohlfart-Kugelberg-Welander disease or hereditary familial spinal juvenile muscular atrophy].[例沃夫哈特-屈尔贝里-韦兰德病或遗传性家族性脊髓性少年型肌萎缩症]

Minerva Med. 1977 Feb 4;68(6):417-24.

[Kugelberg-Welander disease].[库格尔贝格-韦兰德病]

Naika. 1971;28(3):456-7.

[Pseudomyopathical forms of spinal amyotrophy (Kugelberg-Welander disease)].[脊髓性肌萎缩的假肌病形式（库格尔贝格 - 韦兰德病）]

Zh Nevropatol Psikhiatr Im S S Korsakova. 1971;71(8):1139-44.

[Histological changes in the muscles in Kugelberg-Welander disease].[脊髓性肌萎缩症（Kugelberg-Welander病）肌肉的组织学变化]

Zh Nevropatol Psikhiatr Im S S Korsakova. 1974;74(3):346-8.

引用本文的文献

[Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl)].[腓骨肌萎缩症（夏科-马里-图思病）时骨骼肌的线粒体变化。组织学和电子显微镜研究（作者译）]

J Neurol. 1975;209(1):9-29. doi: 10.1007/BF00312522.

本文引用的文献

Cross-innervated mammalian skeletal muscle: histochemical, physiological and biochemical observations.交叉支配的哺乳动物骨骼肌：组织化学、生理学及生物化学观察

J Physiol. 1967 Dec;193(3):481-496.3. doi: 10.1113/jphysiol.1967.sp008373.

Motor unit types of cat triceps surae muscle.猫小腿三头肌的运动单位类型。

J Physiol. 1967 Nov;193(1):141-60. doi: 10.1113/jphysiol.1967.sp008348.

Neurogenic muscular atrophy simulating muscular dystrophy.模拟肌营养不良的神经源性肌肉萎缩

Arch Neurol. 1960 Jun;2:677-82. doi: 10.1001/archneur.1960.03840120083009.

The specificity of the histochemical method for adenosine triphosphatase.三磷酸腺苷酶组织化学方法的特异性。

J Histochem Cytochem. 1955 May;3(3):170-95. doi: 10.1177/3.3.170.

FUNCTIONAL SIGNIFICANCE OF CELL SIZE IN SPINAL MOTONEURONS.脊髓运动神经元中细胞大小的功能意义

J Neurophysiol. 1965 May;28:560-80. doi: 10.1152/jn.1965.28.3.560.

HEREDITARY PROXIMAL NEUROGENIC MUSCULAR ATROPHY IN ADULT.成人遗传性近端神经性肌萎缩

Arch Neurol. 1965 Jun;12:597-603. doi: 10.1001/archneur.1965.00460300045005.

THE WOHLFART-KUGELBERG-WELANDER DISEASE; REVIEW OF THE LITERATURE AND REPORT OF A CASE.沃夫哈特-库格勒贝格-韦兰德病；文献综述及病例报告

Neurology. 1965 May;15:469-73. doi: 10.1212/wnl.15.5.469.

PROPERTIES OF MOTOR UNITS IN A HETEROGENEOUS PALE MUSCLE (M. GASTROCNEMIUS) OF THE CAT.猫的异质性浅色肌肉（腓肠肌）中运动单位的特性

J Neurophysiol. 1965 Jan;28:85-99. doi: 10.1152/jn.1965.28.1.85.

PROPERTIES OF MOTOR UNITS IN A HOMOGENEOUS RED MUSCLE (SOLEUS) OF THE CAT.猫的均匀红色肌肉（比目鱼肌）中运动单位的特性

J Neurophysiol. 1965 Jan;28:71-84. doi: 10.1152/jn.1965.28.1.71.

HISTOCHEMISTRY OF MUSCLE IN INFANTILE SPINAL MUSCULAR ATROPHY.婴儿型脊髓性肌萎缩症的肌肉组织化学

Neurology. 1963 Dec;13:1059-66. doi: 10.1212/wnl.13.12.1059.

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