Publikationen bis 2000

  • A placebo-controlled crossover trial of creatine in mitochondrial diseases. (Neurology)
    Klopstock T, Querner V, Schmidt F, Gekeler F, Walter M, Hartard M, Henning M, Gasser T, Pongratz D, Straube A, Dieterich M, Müller-Felber W
  • Inflammatory myopathy in POEMS syndrome. (Neurology)
    Goebels N, Walther EU, Schaller M, Pongratz D, Mueller-Felber W
  • German open label trial of riluzole 50 mg b.i.d. in treatment of amyotrophic lateral sclerosis (ALS). (J Neurol Sci)
    Pongratz D, Neundörfer B, Fischer W
  • Technology evaluation: edrecolomab, Centocor Inc. (Curr Opin Mol Ther)
    Abicht A, Lochmüller H
  • Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study. (Neurology)
    Walter MC, Lochmüller H, Reilich P, Klopstock T, Huber R, Hartard M, Hennig M, Pongratz D, Müller-Felber W
  • Successful management of polyneuropathy associated with IgM gammopathy of undetermined significance with antibody-based immunoadsorption. (Clin Nephrol)
    Toepfer M, Schroeder M, Müller-Felber W, Lochmüller H, Sitter T, Pongratz D, Schiffl H
  • [Inflammatory myopathies from neurologist's perspective] (Internist (Berl))
    Pongratz D
  • [Peripheral neuropathy in diabetes mellitus from neurological perspective] (Internist (Berl))
    Müller-Felber W
  • [Internal medicine and peripheral neurology] (Internist (Berl))
    Scriba PC, Pongratz D
  • Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients. (Hum Mol Genet)
    Börner GV, Zeviani M, Tiranti V, Carrara F, Hoffmann S, Gerbitz KD, Lochmüller H, Pongratz D, Klopstock T, Melberg A, Holme E, Pääbo S
  • A modified alignment of human and rodent 5' untranslated sequences of the acetylcholine receptor epsilon subunit gene reveals additional regions of high homology. (Neuromuscul Disord)
    Stucka R, Abicht A, Song IH, Bönsch D, Deufel T, Lochmüller H
  • An inherited 4q35-EcoRI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD). (Neuromuscul Disord)
    Busse K, Köhler J, Stegmann K, Pongratz D, Koch MC, Schreiber H
  • Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNS. (J Neurol)
    Horváth R, Abicht A, Shoubridge EA, Karcagi V, Rózsa C, Komoly S, Lochmüller H
  • High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study. (J Neurol)
    Walter MC, Lochmüller H, Toepfer M, Schlotter B, Reilich P, Schröder M, Müller-Felber W, Pongratz D
  • The challenge of fibromyalgia: new approaches. (Scand J Rheumatol Suppl)
    Müller W, Pongratz D, Bärlin E, Eich W, Färber L, Haus U, Lautenschläger J, Mense S, Neeck G, Offenbächer M, Späth M, Stratz T, Tolk J, Welzel D, Wiech K, Wohlgemuth M
  • Efficacy and tolerability of tropisetron in primary fibromyalgia--a highly selective and competitive 5-HT3 receptor antagonist. German Fibromyalgia Study Group. (Scand J Rheumatol Suppl)
    Färber L, Stratz T, Brückle W, Späth M, Pongratz D, Lautenschläger J, Kötter I, Zöller B, Peter HH, Neeck G, Alten R, Müller W
  • Gastrointestinal dysfunction in amyotrophic lateral sclerosis. (Amyotroph Lateral Scler Other Motor Neuron Disord)
    Toepfer M, Folwaczny C, Klauser A, Riepl RL, Müller-Felber W, Pongratz D
  • Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis. (Neuromuscul Disord)
    Müller-Felber W, Ansevin CF, Ricker K, Müller-Jenssen A, Töpfer M, Goebel HH, Pongratz DE
  • Clindamycin and nicotinic neuromuscular transmission. (Lancet)
    Schulze J, Toepfer M, Schroff KC, Aschhoff S, Remien J, Müller-Felber W, Endres S
  • A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin. (Neurology)
    Abicht A, Stucka R, Karcagi V, Herczegfalvi A, Horváth R, Mortier W, Schara U, Ramaekers V, Jost W, Brunner J, Janssen G, Seidel U, Schlotter B, Müller-Felber W, Pongratz D, Rüdel R, Lochmüller H
  • Technology evaluation: CRIB (CNTF delivery) CytoTherapeutics Inc. (Curr Opin Mol Ther)
    Abicht A, Lochmüller H
  • Neuromyotonia, myocloni, sensory neuropathy and cerebellar symptoms in a patient with antibodies to neuronal nucleoproteins (anti-Hu-antibodies). (Clin Neurol Neurosurg)
    Toepfer M, Schroeder M, Unger JW, Lochmüller H, Pongratz D, Müller-Felber W
  • Detection of humoral rejection in human cardiac allografts by assessing the capillary deposition of complement fragment C4d in endomyocardial biopsies. (J Heart Lung Transplant)
    Behr TM, Feucht HE, Richter K, Reiter C, Spes CH, Pongratz D, Uberfuhr P, Meiser B, Theisen K, Angermann CE
  • Extracorporeal antibody elimination in neuroimmunological diseases. (Ther Apher)
    Toepfer M, Schiffl H, Sitter T, Pongratz D, Müller-Felber W
  • Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL. (J Neurol)
    Mayer M, Straube A, Bruening R, Uttner I, Pongratz D, Gasser T, Dichgans M, Müller-Höcker J
  • The diagnostic process in ALS. (J Neurol Sci)
    Pongratz D
  • Phenotypic variability in two brothers with sarcotubular myopathy. (J Neurol)
    Müller-Felber W, Schlotter B, Töpfer M, Ketelsen UP, Müller-Höcker J, Pongratz D
  • Localization of transforming growth factor beta in association with neuromuscular junctions in adult human muscle. (Cell Mol Neurobiol)
    Toepfer M, Fischer P, Abicht A, Lochmüller H, Pongratz D, Müller-Felber W
  • Neurophysiological testing in long-standing cystinosis. (Electromyogr Clin Neurophysiol)
    Müller-Felber W, Schröder M, Hirschmann M, Kastrup K, Töpfer M, Pongratz D
  • Markedly different course of Friedreich's ataxia in sib pairs with similar GAA repeat expansions in the frataxin gene. (Acta Neuropathol (Berl))
    Klopstock T, Chahrokh-Zadeh S, Holinski-Feder E, Meindl A, Gasser T, Pongratz D, Müller-Felber W
  • Myotonic ADR-MDX mutant mice show less severe muscular dystrophy than MDX mice. (Neuromuscul Disord)
    Krämer R, Lochmüller H, Abicht A, Rüdel R, Brinkmeier H
  • Metastasis of carcinoma to skeletal muscle leading to myosclerosis and progressive contractures. (J Neurol)
    Klopstock T, Haberl RL, Hundt W, Pongratz D
  • Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene. (Ann Neurol)
    Jaksch M, Klopstock T, Kurlemann G, Dörner M, Hofmann S, Kleinle S, Hegemann S, Weissert M, Müller-Höcker J, Pongratz D, Gerbitz KD
  • Incidence of humoral rejection in heart transplant recipients treated with tacrolimus or cyclosporine A. (Transplant Proc)
    Behr TM, Richter K, Fischer P, Spes CH, Meiser B, Reichart B, Pongratz D, Feucht H, Theisen K, Angermann CE
  • Tenascin is a useful marker in the diagnosis of inflammatory myopathies. (Eur J Med Res)
    Müller-Felber W, Toepfer M, Müller T, Müller-Höcker J, Fischer P, Lochmüller H, Pongratz D
  • Drug-induced systemic lupus erythematosus after 8 years of treatment with carbamazepine. (Eur J Clin Pharmacol)
    Toepfer M, Sitter T, Lochmüller H, Pongratz D, Müller-Felber W
  • Marinesco Sjögren syndrome with rhabdomyolysis. A new subtype of the disease. (Neuropediatrics)
    Müller-Felber W, Zafiriou D, Scheck R, Pätzke I, Toepfer M, Pongratz DE, Walther U
  • Mutation analysis in myophosphorylase deficiency (McArdle's disease). (Ann Neurol)
    Vorgerd M, Kubisch C, Burwinkel B, Reichmann H, Mortier W, Tettenborn B, Pongratz D, Lindemuth R, Tegenthoff M, Malin JP, Kilimann MW
  • Rapidly progredient scoliosis associated with multicore disease. (Arch Orthop Trauma Surg)
    Pellengahr C, Krödel A, Müller-Höcker J, Pongratz D
  • Changes of sonographic, magnetic resonance tomographic, electromyographic, and histopathologic findings within a 2-month period of examinations after experimental muscle denervation. (Arch Orthop Trauma Surg)
    Küllmer K, Sievers KW, Reimers CD, Rompe JD, Müller-Felber W, Nägele M, Harland U
  • Congenital myasthenic syndromes: clinical and genetic analysis of 18 patients. (Eur J Med Res)
    Abicht A, Müller-Felber W, Fischer P, Jakob I, Kürz L, Rudel R, Mortier W, Pongratz D, Lochmüller H
  • Delayed colonic transit times in amyotrophic lateral sclerosis assessed with radio-opaque markers. (Eur J Med Res)
    Toepfer M, Schroeder M, Klauser A, Lochmüller H, Hirschmann M, Riepl RL, Pongratz D, Müller-Felber W
  • Upregulation of utrophin in the myocardium of a carrier of Duchenne muscular dystrophy. (Eur Heart J)
    Behr TM, Fischer P, Mudra H, Theisen K, Spes C, Uberfuhr P, Müller-Felber W, Pongratz DE, Angermann C
  • [50-year-old patient with rapid ataxia onset, generalized paresthesia and myoclonus] (Internist (Berl))
    Toepfer M, Müller-Felber W, Huber RM, Held E, Wekerle G, Unger J, Schlotter B, Pongratz D
  • [Recommendations of Bavarian Muscle Centers of the German Neuromuscular Disease Society for home ventilation of neuromuscular diseases of adult patients] (Nervenarzt)
    Winterholler M, Claus D, Bockelbrink A, Borasio GD, Pongratz D, Schrank B, Toyka KV, Neundörfer B
  • Differential expression of perforin in muscle-infiltrating T cells in polymyositis and dermatomyositis. (J Clin Invest)
    Goebels N, Michaelis D, Engelhardt M, Huber S, Bender A, Pongratz D, Johnson MA, Wekerle H, Tschopp J, Jenne D, Hohlfeld R
  • Annexin VII relocalization as a result of dystrophin deficiency. (Exp Cell Res)
    Selbert S, Fischer P, Menke A, Jockusch H, Pongratz D, Noegel AA
  • Electrophysiological characterization of nicotinic receptors of aneurally grown human myotubes. (Neurosci Lett)
    Bufler J, Fischer P, Pongratz D, Franke C
  • [Paresthesia] (Internist (Berl))
    Müller-Felber W, Pongratz D
  • Duct occlusion-induced vascularized islet grafts are not associated with progressive long-term dysfunction. (Transplant Proc)
    Illner WD, Schneeberger H, Hofmann G, Piehlmeier W, Mojto J, Scheuer R, Müller-Felber W, Landgraf R, Land W
  • Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy. (Arch Neurol)
    Ricker K, Koch MC, Lehmann-Horn F, Pongratz D, Speich N, Reiners K, Schneider C, Moxley RT
  • Expression and localization of annexin VII (synexin) in muscle cells. (J Cell Sci)
    Selbert S, Fischer P, Pongratz D, Stewart M, Noegel AA
  • [Rhabdomyolysis in neuroleptic therapy: an abortive malignant neuroleptic syndrome?] (Nervenarzt)
    Peschel O, Kurtz G, Müller-Felber W, Modell S
  • Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts. (Neurology)
    Ricker K, Koch MC, Lehmann-Horn F, Pongratz D, Otto M, Heine R, Moxley RT
  • Myofibrillogenesis in primary tissue cultures of adult human skeletal muscle: expression of desmin, titin, and nebulin. (Clin Investig)
    Behr T, Fischer P, Müller-Felber W, Schmidt-Achert M, Pongratz D
  • Diabetic neuropathy 3 years after successful pancreas and kidney transplantation. (Diabetes)
    Müller-Felber W, Landgraf R, Scheuer R, Wagner S, Reimers CD, Nusser J, Abendroth D, Illner WD, Land W
  • [Endogenous bilateral compression syndrome of the suprascapular nerve. Overview and case report] (Nervenarzt)
    Heuss D, Lochmüller H, Habermeyer P, Reimers C, Pongratz D
  • Combined ultrasonographic and neurographic examination: a new technique to evaluate phrenic nerve function. (Electromyogr Clin Neurophysiol)
    Müller-Felber W, Riepl R, Reimers CD, Wagner S, Pongratz D
  • Myositis in Lyme borreliosis: an immunohistochemical study of seven patients. (J Neurol Sci)
    Müller-Felber W, Reimers CD, de Koning J, Fischer P, Pilz A, Pongratz DE
  • Myoadenylate deaminase deficiency with severe rhabdomyolysis. (Eur J Pediatr)
    Baumeister FA, Gross M, Wagner DR, Pongratz D, Eife R
  • Borrelia burgdorferi myositis: report of eight patients. (J Neurol)
    Reimers CD, de Koning J, Neubert U, Preac-Mursic V, Koster JG, Müller-Felber W, Pongratz DE, Duray PH
  • Muscular ultrasound in idiopathic inflammatory myopathies of adults. (J Neurol Sci)
    Reimers CD, Fleckenstein JL, Witt TN, Müller-Felber W, Pongratz DE
  • Heterozygotic gene expression in endomyocardial biopsies: a new diagnostic tool confirms the Duchenne carrier status. (Clin Investig)
    Schmidt-Achert M, Fischer P, Müller-Felber W, Mudra H, Pongratz D
  • Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency. (Arch Pathol Lab Med)
    Müller-Höcker J, Hübner G, Bise K, Förster C, Hauck S, Paetzke I, Pongratz D, Kadenbach B
  • The clinical spectrum of Friedreich's ataxia in German families showing linkage to the FRDA locus on chromosome 9. (Clin Investig)
    Müller-Felber W, Rossmanith T, Spes C, Chamberlain S, Pongratz D, Deufel T
  • High incidence of carpal tunnel syndrome in diabetic patients after combined pancreas and kidney transplantation. (Acta Diabetol)
    Müller-Felber W, Landgraf R, Reimers CD, Scheuer R, Wagner S, Nusser J, Abendroth A, Illner WD, Land W
  • Cross-sectional study of peripheral microcirculation in diabetic patients with microangiopathy: influence of pancreatic and kidney transplantation. (Acta Diabetol)
    Gfesser M, Nusser J, Müller-Felber W, Abendroth D, Land W, Landgraf R
  • Fibre type specific expression of Leu19-antigen and N-CAM in skeletal muscle in various stages after experimental denervation. (Virchows Arch A Pathol Anat Histopathol)
    Müller-Felber W, Küllmer K, Fischer P, Reimers CD, Wagner S, Harland U, Schmidt-Achert M, Pongratz D
  • Myocardial evidence of dystrophin mosaic in a Duchenne muscular dystrophy carrier. (Lancet)
    Schmidt-Achert M, Fischer P, Pongratz D
  • Molecular basis of AMP deaminase deficiency in skeletal muscle. (Proc Natl Acad Sci U S A)
    Morisaki T, Gross M, Morisaki H, Pongratz D, Zöllner N, Holmes EW
  • Evidence for genetic heterogeneity of malignant hyperthermia susceptibility. (Am J Hum Genet)
    Deufel T, Golla A, Iles D, Meindl A, Meitinger T, Schindelhauer D, DeVries A, Pongratz D, MacLennan DH, Johnson KJ
  • Mitochondrial angiopathy in a family with MELAS. (Neuropediatrics)
    Förster C, Hübner G, Müller-Höcker J, Pongratz D, Baierl P, Senger R, Ruitenbeek W
  • [Inflammatory muscle diseases. International symposium "Inflammatory myopathies", Munich 26 September 1991] (Med Klin (Munich))
    Pongratz D, Reimers CD, Schmidt-Achert M
  • Subcellular distribution of GLUT 4 in the skeletal muscle of lean type 2 (non-insulin-dependent) diabetic patients in the basal state. (Diabetologia)
    Vogt B, Mühlbacher C, Carrascosa J, Obermaier-Kusser B, Seffer E, Mushack J, Pongratz D, Häring HU
  • [Tremor] (Internist (Berl))
    Müller-Felber W, Pongratz D
  • Chronic myopathy in a patient suspected of carrying two malignant hyperthermia susceptibility (MHS) mutations. (Neuromuscul Disord)
    Deufel T, Müller-Felber W, Pongratz DE, Hübner G, Johnson K, Iaizzo PA, Lehmann-Horn F
  • [A paranoid syndrome after discontinuing tuberculostatics] (Dtsch Med Wochenschr)
    Müller N, Günther W, Müller-Felber W
  • A specific point mutation in the mitochondrial genome of Caucasians with MELAS. (Hum Genet)
    Enter C, Müller-Höcker J, Zierz S, Kurlemann G, Pongratz D, Förster C, Obermaier-Kusser B, Gerbitz KD
  • Follow-up study of sensory-motor polyneuropathy in type 1 (insulin-dependent) diabetic subjects after simultaneous pancreas and kidney transplantation and after graft rejection. (Diabetologia)
    Müller-Felber W, Landgraf R, Wagner S, Mair N, Nusser J, Landgraf-Leurs MM, Abendroth A, Illner WD, Land W
  • Morphology of the diaphragmatic muscle in CDH. (Eur J Pediatr Surg)
    Dietz HG, Pongratz D
  • Type 2a fibre rhabdomyolysis in myoadenylate deaminase deficiency. (J Neurol)
    Zimmer C, Altenkirch H, Dorfmüller-Küchlin S, Pongratz D, Paetzke I, Gosztonyi G
  • [Pancreas transplantation in Type I diabetic patients] (Fortschr Med)
    Landgraf R, Nusser J, Müller-Felber W, Wagner S, Scheider A, Meyer-Schwickerath E, Illner WD, Abendroth D, Land W
  • Normal restriction pattern (Hind III) of the myoadenylate deaminase gene in enzyme deficient patients. (Klin Wochenschr)
    Gross M, Morisaki T, Pongratz D, Holmes EW, Zöllner N
  • [Paraneoplastic myopathies] (Internist (Berl))
    Pongratz D, Müller-Felber W
  • [Muscular pain] (Internist (Berl))
    Pongratz D, Müller-Felber W
  • Mutations of the mitochondrial DNA: the contribution of DNA techniques to the diagnosis of mitochondrial encephalomyopathies. (J Clin Chem Clin Biochem)
    Gerbitz KD, Obermaier-Kusser B, Lestienne P, Zierz S, Müller-Höcker J, Pongratz D, Paetzke-Brunner I, Deufel T
  • Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes. (J Neurol)
    Gerbitz KD, Obermaier-Kusser B, Zierz S, Pongratz D, Müller-Höcker J, Lestienne P
  • [Manifestations in skeletal muscle] (Verh Dtsch Ges Inn Med)
    Pongratz D
  • Metabolic control and effect on secondary complications of diabetes mellitus by pancreatic transplantation. (Baillieres Clin Gastroenterol)
    Landgraf R, Nusser J, Scheuer R, Fiedler A, Scheider A, Meyer-Schwickerath E, Müller-Felber W, Illner WD, Abendroth D, Land W
  • Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study. (Hum Pathol)
    Müller-Höcker J, Droste M, Kadenbach B, Pongratz D, Hübner G
  • [Muscle pain in myopathies] (Verh Dtsch Ges Inn Med)
    Pongratz D
  • [Subcutaneous vascular access] (Z Urol Nephrol)
    Heinrich P, Müller JS
  • Autosomal dominant Emery-Dreifuss syndrome: evidence of a neurogenic variant of the disease. (Eur Arch Psychiatry Neurol Sci)
    Witt TN, Garner CG, Pongratz D, Baur X
  • [Diagnosis of susceptibility to malignant hyperthermia using the in vitro contracture test] (Anaesthesist)
    Klein W, Spiess-Kiefer C, Küther G, Pongratz D, Lehmann-Horn F
  • [Dominant autosomal humeroperoneal syndrome with early contractures and cardiomyopathy (Emery-Dreifuss syndrome)] (Klin Wochenschr)
    Baur X, Witt TN, Pongratz D, Gokel M, Rosenbeiger P, Steinbeck G
  • [Gilles de la Tourette syndrome and spinal muscular atrophy of the peroneal type. A case report] (Nervenarzt)
    Schölderle M, Greil W, Pongratz D
  • Congestive heart failure due to mitochondrial cardiomyopathy in Kearns-Sayre syndrome. (Klin Wochenschr)
    Kleber FX, Park JW, Hübner G, Johannes A, Pongratz D, König E
  • Myoadenylate deaminase deficiency: successful symptomatic therapy by high dose oral administration of ribose. (Klin Wochenschr)
    Zöllner N, Reiter S, Gross M, Pongratz D, Reimers CD, Gerbitz K, Paetzke I, Deufel T, Hübner G
  • [Superfluous diagnosis? Status of muscle biopsy of collagenoses] (Internist (Berl))
    Pongratz D, Burg D
  • [Cardiac manifestation of progressive muscular dystrophy of the Duchenne type] (Z Kardiol)
    Angermann C, Spes C, Pongratz D
  • Activation of mitochondrial ATPase as evidence of loosely coupled oxidative phosphorylation in various skeletal muscle disorders. A histochemical fine-structural study. (J Neurol Sci)
    Müller-Höcker J, Pongratz D, Hübner G
  • Fatal mitochondrial cardiomyopathy in Kearns-Sayre syndrome. (Virchows Arch A Pathol Anat Histopathol)
    Hübner G, Gokel JM, Pongratz D, Johannes A, Park JW
  • Fatal mitochondrial cardiomyopathy in Kearns-Sayre syndrome with deficiency of cytochrome-c-oxidase in cardiac and skeletal muscle. An enzymehistochemical--ultra-immunocytochemical--fine structural study in longterm frozen autopsy tissue. (Virchows Arch B Cell Pathol Incl Mol Pathol)
    Müller-Höcker J, Johannes A, Droste M, Kadenbach B, Pongratz D, Hübner G
  • Mitochondrial myopathy with diffuse activation and focal deficiency of mitochondrial ATPase and carnitine deficiency. (Virchows Arch B Cell Pathol Incl Mol Pathol)
    Müller-Höcker J, Paetzke I, Pongratz D, Hübner G
  • [Morphology of metabolic myopathies] (Monatsschr Kinderheilkd)
    Pongratz D, Hübner G
  • [Diagnostic significance of muscle biopsies in metabolic myopathies. II. Clinical biochemistry] (Klin Wochenschr)
    Deufel T, Paetzke I, Pongratz D, Hübner G, Wieland OH
  • Myopathic carnitine deficiency associated with lymphocytic malignant non-Hodgkin lymphoma and monoclonal immunoglobulin G-K. (Klin Wochenschr)
    Deufel T, Siegert W, Pongratz D, Jacob K, Wieland OH
  • [Diagnostic significance of muscle biopsies in metabolic myopathies. I. Myopathology] (Klin Wochenschr)
    Pongratz D, Hübner G, Deufel T, Paetzke I, Wieland OH
  • [Adult form of acid maltase deficiency presenting as progressive spinal muscular atrophy] (Dtsch Med Wochenschr)
    Pongratz D, Kötzner H, Hübner G, Deufel T, Wieland OH
  • Mitochondrial myopathy with loosely coupled oxidative phosphorylation in a case of Zellweger syndrome. A cytochemical-ultrastructural study. (Virchows Arch B Cell Pathol Incl Mol Pathol)
    Müller-Höcker J, Walther JU, Bise K, Pongratz D, Hübner G
  • [Mitigated adult forms of acid maltase deficiency (Pompe's disease). Morphologic and pathobiochemical studies] (Klin Wochenschr)
    Pongratz D, Hübner G, Deufel T, Wieland OH
  • [Glycogenosis type V (McArdle)--epilepsy--congenital cataracts in retinitis pigmentosa. A new syndrome?] (Nervenarzt)
    Spatz R, Wolf B, Pongratz D
  • Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia. Cytochemical-fine-structural study. (Virchows Arch A Pathol Anat Histopathol)
    Müller-Höcker J, Pongratz D, Hübner G
  • 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. (Virchows Arch A Pathol Anat Histopathol)
    Müller-Höcker J, Pongratz D, Deufel T, Trijbels JM, Endres W, Hübner G
  • [Fasciitis and eosinophilia--a scleroderma-like disease] (Internist (Berl))
    Koppenwallner C, Pongratz D
  • [Granular body myopathy (so-called reducing body myopathy)] (Pathologe)
    Hübner G, Pongratz D
  • Pseudohypoparathyroidism and hypocalcemic "myopathy". A case report. (Klin Wochenschr)
    Piechowiak H, Gröbner W, Kremer H, Pongratz D, Schaub J
  • [Morphological and biochemical studies on glycogenosis type V (McArdle) (author's transl)] (Klin Wochenschr)
    Pongratz D, Schaub J, Koppenwallner C, Hübner G
  • [Reducing body myopathy--ultrastructure and classification (author's transl)] (Virchows Arch A Pathol Anat Histol)
    Hübner G, Pongratz D
  • [Ultrastructural and clinical studies in "inclusion body myositis" (author's transl)] (Fortschr Neurol Psychiatr Grenzgeb)
    Lisson G, Pongratz D, Hübner G, Wallesch C
  • [Value of myometric findings in the morphological differential diagnosis of neuromuscular disorders (author's transl)] (Microsc Acta Suppl)
    Pongratz D
  • [Mucopolysaccharidosis I-S (Scheie's disease) (author's transl)] (Dtsch Med Wochenschr)
    Luderschmidt C, Schill WB, Burg D, von Figura K, Hübner G, Pongratz D
  • [Clinical, morphological and biochemical studies on muscle carnitine deficiency (author's transl)] (Klin Wochenschr)
    Pongratz D, Hübner G, Deufel T, Wieland O, Pongratz E, Liphardt R
  • [Muscle biopsy in progressive external ophthalmoplegia (author's transl)] (Klin Wochenschr)
    Pongratz D, Perwein J, Hübner G, Koppenwallner C, Toyka K, Birnberger KL
  • [Sarciodosis. Neurologic organ manifestation--a case contribution] (MMW Munch Med Wochenschr)
    Pongratz D, Burg D
  • [Diagnostic value of muscle biopsy findings in myotonic dystrophy (Curschmann-Steinert) (author's transl)] (Klin Wochenschr)
    Pongratz D, Schultz D, Koppenwallner C, Hübner G
  • [Muscle flaccidity as a leading and warning symptom in endocrinopathies] (Verh Dtsch Ges Inn Med)
    Pongratz D, Scriba PC
  • [Differential diagnosis of the inflammatory reactions in the muscle vascular connective tissue apparatus in rheumatic diseases] (Verh Dtsch Ges Rheumatol)
    Pongratz D
  • Prenatal diagnosis of Duchenne's muscular dystrophy. (Lancet)
    Stengel-Rutkowski L, Scheuerbrandt G, Beckmann R, Pongratz D
  • [Congenital centronuclear myopathy. Two morphological variants in one family (author's transl)] (Klin Wochenschr)
    Pongratz D, Weindl A, Reichl W, Koppenwallner C, Heuser M, Hübner G
  • [Central core disease with "structured cores" in type II-fibers (author's transl)] (Klin Wochenschr)
    Pongratz D, Heuser M, Koppenwallner C, Hübner G
  • An especially mild myopathic form of glycogenosis type II. Problems of clinical and light microscopic diagnosis. (Pathol Eur)
    Pongratz D, Schlossmacher I, Koppenwallner C, Hübner G
  • [Polyneuritis and Landry's paralysis (author's transl)] (MMW Munch Med Wochenschr)
    Spatz R, Jordan H, Weller E, Pongratz D, Haider M
  • [Opthalmoplegia externa progressiva. A clinical and morphological study (author's transl)] (Z Neurol)
    Birnberger KL, Weindl A, Struppler A, Schinko I, Pongratz D
  • [Muscle biopsy in the diagnosis of neuromuscular diseases] (Internist (Berl))
    Mittelbach F, Pongratz D
  • [Histochemical evidence of leucine aminopeptidase activity in human skeletal muscle in myopathies] (Virchows Arch A Pathol Pathol Anat)
    Mittelbach F, Pongratz D
  • [Immunochemical studies in various human myopathies] (Virchows Arch A Pathol Pathol Anat)
    Mittelbach F, Pongratz D
  • [Treatment of the myasthenic syndrome with Mestinon retard] (Munch Med Wochenschr)
    Mittelbach F, Pongratz D
  • [Clinical, histological and histochemical studies in a case of central core disease (central fibrillar myopathy)] (Dtsch Z Nervenheilkd)
    Mittelbach F, Pongratz D
  • [Studies on histochemical demonstration of potassium in skeletal muscle] (Histochemie)
    Mittelbach F, Pongratz D
  • [Fluorescence immunohistochemical determination of creatine phosphokinase in the skeletal muscle of rabbit and man] (Z Gesamte Exp Med)
    Mittelbach F, Pongratz D
  • [Histological and histochemical studies on the influence of prednisolone acetate on the normal and denervated skeletal muscle of the mouse] (Virchows Arch Pathol Anat Physiol Klin Med)
    Mittelbach F, Pongratz D
  • [On the effect of anabolic steroids on normal and denervated muscle] (Virchows Arch Pathol Anat Physiol Klin Med)
    Pongratz D, Mittelbach F