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Results of search for 'au:"Müller-Hocker, J"', page 6 of 7
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Authors
Belohradsky, B H
Bise, K
Brenner, P
Deufel, T
Dichgans, M
Gerbitz, K D
Hammer, C
Horvath, R
Horváth, R
Hübner, G
Jaksch, M
Kadenbach, B
Lochmüller, H
Müller-Höcker, J
Münscher, C
Obermaier-Kusser, B
Pongratz, D
Schäfer, S
Seibel, P
Weiss, M
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DNA, Mitochondrial
Electron Transport Complex IV
Female
Humans
Immunohistochemistry
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Microscopy, Electron
Middle Aged
Mutation
analysis
diagnosis
enzymology
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Your search returned 134 results.
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101.
Aggressive scapular chondroblastoma with secondary metastasis--a case report and review of literature.
[electronic resource]
by
Kirchhoff, C
Buhmann, S
Mussack, T
Müller-Höcker, J
Schmitt-Sody, M
Jansson, V
Dürr, H-R
Producer:
20060630
In:
European journal of medical research
vol. 11
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102.
Paraneoplastic chronic intestinal pseudoobstruction as a rare complication of bronchial carcinoid.
[electronic resource]
by
Gerl, A
Storck, M
Schalhorn, A
Müller-Höcker, J
Jauch, K W
Schildberg, F W
Wilmanns, W
Producer:
19920908
In:
Gut
vol. 33
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103.
In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathy.
[electronic resource]
by
Müller-Höcker, J
Seibel, P
Schneiderbanger, K
Zietz, C
Obermaier-Kusser, B
Gerbitz, K D
Kadenbach, B
Producer:
19930127
In:
Human pathology
vol. 23
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104.
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.
[electronic resource]
by
Müller-Höcker, J
Hübner, G
Bise, K
Förster, C
Hauck, S
Paetzke, I
Pongratz, D
Kadenbach, B
Producer:
19930304
In:
Archives of pathology & laboratory medicine
vol. 117
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105.
Congenital alveolar capillary dysplasia: rare cause of persistent pulmonary hypertension.
[electronic resource]
by
Haraida, S
Lochbühler, H
Heger, A
Nerlich, A
Diebold, J
Wiest, I
Müller-Höcker, J
Löhrs, U
Producer:
19971209
In:
Pediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association
vol. 17
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106.
[Somnolence and vomiting in a patient after parathyroid gland carcinoma surgery].
[electronic resource]
by
Geier, A
Fürst, H
Laubach, E
Stäbler, A
Tiling, R
Müller-Höcker, J
Schwandt, P
Ritter, M M
Producer:
19990810
In:
Der Internist
vol. 40
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107.
Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited.
[electronic resource]
by
Schoser, B G H
Müller-Höcker, J
Horvath, R
Gempel, K
Pongratz, D
Lochmüller, H
Müller-Felber, W
Producer:
20071113
In:
Neuropathology and applied neurobiology
vol. 33
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108.
Monoclonal gammopathy after low-grade MALT lymphoma: evidence for a second neoplasm.
[electronic resource]
by
Pachmann, S
Anderegg, B
Müller-Höcker, J
Nathrath, W
Brack, N
Tigges, F J
Hartenstein, R
Munker, R
Producer:
20020731
In:
American journal of hematology
vol. 70
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109.
Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies.
[electronic resource]
by
Müller-Höcker, J
Ibel, H
Paetzke, I
Deufel, T
Endres, W
Kadenbach, B
Gokel, J M
Hübner, G
Producer:
19911213
In:
Virchows Archiv. A, Pathological anatomy and histopathology
vol. 419
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110.
Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNA(Leu(UUR))].
[electronic resource]
by
Obermaier-Kusser, B
Paetzke-Brunner, I
Enter, C
Müller-Höcker, J
Zierz, S
Ruitenbeek, W
Gerbitz, K D
Producer:
19910909
In:
FEBS letters
vol. 286
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111.
Defects of the respiratory chain in oxyphil and chief cells of the normal parathyroid and in hyperfunction.
[electronic resource]
by
Müller-Höcker, J
Aust, D
Napiwotzky, J
Münscher, C
Link, T A
Seibel, P
Schneeweiss, S G
Kadenbach, B
Producer:
19960805
In:
Human pathology
vol. 27
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112.
A specific point mutation in the mitochondrial genome of Caucasians with MELAS.
[electronic resource]
by
Enter, C
Müller-Höcker, J
Zierz, S
Kurlemann, G
Pongratz, D
Förster, C
Obermaier-Kusser, B
Gerbitz, K D
Producer:
19920204
In:
Human genetics
vol. 88
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113.
Renal Fanconi syndrome: first sign of partial respiratory chain complex IV deficiency.
[electronic resource]
by
Kuwertz-Bröking, E
Koch, H G
Marquardt, T
Rossi, R
Helmchen, U
Müller-Höcker, J
Harms, E
Bulla, M
Producer:
20001011
In:
Pediatric nephrology (Berlin, Germany)
vol. 14
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114.
Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic study.
[electronic resource]
by
Müller-Höcker, J
Horvath, R
Schäfer, S
Hessel, H
Müller-Felber, W
Kühr, J
Copeland, W C
Seibel, P
Producer:
20120416
In:
Journal of cellular and molecular medicine
vol. 15
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115.
The phenotypic spectrum of CADASIL: clinical findings in 102 cases.
[electronic resource]
by
Dichgans, M
Mayer, M
Uttner, I
Brüning, R
Müller-Höcker, J
Rungger, G
Ebke, M
Klockgether, T
Gasser, T
Producer:
19981202
In:
Annals of neurology
vol. 44
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116.
Mutations of the mitochondrial DNA: the contribution of DNA techniques to the diagnosis of mitochondrial encephalomyopathies.
[electronic resource]
by
Gerbitz, K D
Obermaier-Kusser, B
Lestienne, P
Zierz, S
Müller-Höcker, J
Pongratz, D
Paetzke-Brunner, I
Deufel, T
Producer:
19900801
In:
Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie
vol. 28
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117.
Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome.
[electronic resource]
by
Heymans, H S
vd Bosch, H
Schutgens, R B
Tegelaers, W H
Walther, J U
Müller-Höcker, J
Borst, P
Producer:
19840611
In:
European journal of pediatrics
vol. 142
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118.
Defects of the respiratory chain in the normal human liver and in cirrhosis during aging.
[electronic resource]
by
Müller-Höcker, J
Aust, D
Rohrbach, H
Napiwotzky, J
Reith, A
Link, T A
Seibel, P
Hölzel, D
Kadenbach, B
Producer:
19971008
In:
Hepatology (Baltimore, Md.)
vol. 26
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119.
Benign symmetric lipomatosis with axonal neuropathy and abnormalities in specific mitochondrial tRNA regions.
[electronic resource]
by
Gdynia, Hans-Jürgen
Sperfeld, A-D
Knirsch, U
Homberg, V
Rosenbohm, A
Müller-Höcker, J
Ludolph, A C
Hanemann, C O
Producer:
20070702
In:
European journal of medical research
vol. 11
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120.
Transgenic human decay accelerating factor makes normal pigs function as a concordant species.
[electronic resource]
by
Schmoeckel, M
Nollert, G
Shahmohammadi, M
Müller-Höcker, J
Young, V K
Kasper-König, W
White, D J
Hammer, C
Reichart, B
Producer:
19970909
In:
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
vol. 16
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