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41 in total

1. Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells.

Authors: H R Scholte; H F Busch; I E Luyt-Houwen; M H Vaandrager-Verduin; H Przyrembel; W F Arts
Journal: J Inherit Metab Dis Date: 1987 Impact factor: 4.982

2. Ultrastructural alterations of tissue cultures from human fetal brain infected with the E variant of EMC virus.

Authors: M Adachi; D Amsterdam; S E Brooks; B W Volk
Journal: Acta Neuropathol Date: 1975-08-11 Impact factor: 17.088

3. Acid maltase deficiency: a case study and review of the pathophysiological changes and proposed therapeutic measures.

Authors: H Isaacs; N Savage; M Badenhorst; T Whistler
Journal: J Neurol Neurosurg Psychiatry Date: 1986-09 Impact factor: 10.154

4. Myopathy with mitochondrial abnormalities and rimmed vacuoles.

Authors: J Lehmann; J Ziegan; G Oertel; J Lössner; H J Kühn
Journal: Acta Neuropathol Date: 1986 Impact factor: 17.088

5. Classification of late myopathies based on observation of 15 new cases.

Authors: G Bekény
Journal: Z Neurol Date: 1972

6. Myopathy due to juvenile acid maltase deficiency affecting exclusively the type I fibres.

Authors: T Papapetropoulos; C Paschalis; P Manda
Journal: J Neurol Neurosurg Psychiatry Date: 1984-02 Impact factor: 10.154

7. Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases.

Authors: L Bet; M Moggio; G P Comi; C Mariani; A Prelle; N Checcarelli; A Bordoni; N Bresolin; E Scarpini; G Scarlato
Journal: J Neurol Date: 1994-07 Impact factor: 4.849

8. [Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl)].

Authors: G Spalke; R Heene; D Herold
Journal: J Neurol Date: 1975 Impact factor: 4.849

9. Localization of dystrophin and beta-spectrin in vacuolar myopathies.

Authors: J L De Bleecker; A G Engel; J C Winkelmann
Journal: Am J Pathol Date: 1993-10 Impact factor: 4.307

10. Leaky splicing mutation in the acid maltase gene is associated with delayed onset of glycogenosis type II.

Authors: C F Boerkoel; R Exelbert; C Nicastri; R C Nichols; F W Miller; P H Plotz; N Raben
Journal: Am J Hum Genet Date: 1995-04 Impact factor: 11.025