Deufel T - Search Results

1

Myoadenylate deaminase deficiency: successful symptomatic therapy by high dose oral administration of ribose.

Zöllner N, Reiter S, Gross M, Pongratz D, Reimers CD, Gerbitz K, Paetzke I, Deufel T, Hübner G. Zöllner N, et al. Among authors: deufel t. Klin Wochenschr. 1986 Dec 15;64(24):1281-90. doi: 10.1007/BF01785710. Klin Wochenschr. 1986. PMID: 3102830

2

[Mitigated adult forms of acid maltase deficiency (Pompe's disease). Morphologic and pathobiochemical studies].

Pongratz D, Hübner G, Deufel T, Wieland OH. Pongratz D, et al. Among authors: deufel t. Klin Wochenschr. 1983 Aug 1;61(15):743-50. doi: 10.1007/BF01497401. Klin Wochenschr. 1983. PMID: 6413751 German. No abstract available.

3

[Diagnostic significance of muscle biopsies in metabolic myopathies. II. Clinical biochemistry].

Deufel T, Paetzke I, Pongratz D, Hübner G, Wieland OH. Deufel T, et al. Klin Wochenschr. 1984 Jul 16;62(14):651-8. doi: 10.1007/BF01716461. Klin Wochenschr. 1984. PMID: 6590924 German.

4

[Clinical, morphological and biochemical studies on muscle carnitine deficiency (author's transl)].

Pongratz D, Hübner G, Deufel T, Wieland O, Pongratz E, Liphardt R. Pongratz D, et al. Among authors: deufel t. Klin Wochenschr. 1979 Sep 17;57(18):927-36. doi: 10.1007/BF01478549. Klin Wochenschr. 1979. PMID: 502358 German.

5

Myopathic carnitine deficiency associated with lymphocytic malignant non-Hodgkin lymphoma and monoclonal immunoglobulin G-K.

Deufel T, Siegert W, Pongratz D, Jacob K, Wieland OH. Deufel T, et al. Klin Wochenschr. 1984 Jul 16;62(14):669-74. doi: 10.1007/BF01716463. Klin Wochenschr. 1984. PMID: 6471781

6

[Diagnostic significance of muscle biopsies in metabolic myopathies. I. Myopathology].

Pongratz D, Hübner G, Deufel T, Paetzke I, Wieland OH. Pongratz D, et al. Among authors: deufel t. Klin Wochenschr. 1984 Jul 2;62(13):603-12. doi: 10.1007/BF01721915. Klin Wochenschr. 1984. PMID: 6592394 German.

7

[Adult form of acid maltase deficiency presenting as progressive spinal muscular atrophy].

Pongratz D, Kötzner H, Hübner G, Deufel T, Wieland OH. Pongratz D, et al. Among authors: deufel t. Dtsch Med Wochenschr. 1984 Apr 6;109(14):537-41. doi: 10.1055/s-2008-1069229. Dtsch Med Wochenschr. 1984. PMID: 6368168 German.

8

[Metabolic myopathies].

Pongratz DE, Deufel T. Pongratz DE, et al. Among authors: deufel t. Internist (Berl). 1987 Sep;28(9):590-5. Internist (Berl). 1987. PMID: 3312070 German. No abstract available.

9

Mutations of the mitochondrial DNA: the contribution of DNA techniques to the diagnosis of mitochondrial encephalomyopathies.

Gerbitz KD, Obermaier-Kusser B, Lestienne P, Zierz S, Müller-Höcker J, Pongratz D, Paetzke-Brunner I, Deufel T. Gerbitz KD, et al. Among authors: deufel t. J Clin Chem Clin Biochem. 1990 Apr;28(4):241-50. doi: 10.1515/cclm.1990.28.4.241. J Clin Chem Clin Biochem. 1990. PMID: 2162908

10

Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle.

Müller-Höcker J, Pongratz D, Deufel T, Trijbels JM, Endres W, Hübner G. Müller-Höcker J, et al. Among authors: deufel t. Virchows Arch A Pathol Anat Histopathol. 1983;399(1):11-23. doi: 10.1007/BF00666215. Virchows Arch A Pathol Anat Histopathol. 1983. PMID: 6298999

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