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MesP1 drives vertebrate cardiovascular differentiation through Dkk-1-mediated blockade of Wnt-signalling

Nature cell biology, 2008-03, Vol.10 (3), p.338-345

2008

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Chloroquine-induced phospholipidosis of the kidney mimicking fabry's disease: Case report and review of the literature

Human pathology, 2003-03, Vol.34 (3), p.285-289

2003

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Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study

The American journal of pathology, 1989-05, Vol.134 (5), p.1167-1173

Muller-Hocker, J

1989

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De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy

Neuromuscular disorders : NMD, 2002-12, Vol.12 (10), p.947-951

2002

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A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy

Journal of medical genetics, 2003-10, Vol.40 (10), p.752

2003

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Renal Fanconi syndrome: first sign of partial respiratory chain complex IV deficiency

Pediatric nephrology (Berlin, West), 2000-06, Vol.14 (6), p.495-498

2000

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Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Journal of medical genetics, 2004-11, Vol.41 (11), p.842-848

2004

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Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene

Annals of neurology, 1998-10, Vol.44 (4), p.635-640

1998

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Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies

Journal of medical genetics, 2001-10, Vol.38 (10), p.665-673

2001

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Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts

Human molecular genetics, 2001-12, Vol.10 (26), p.3025-3035

2001

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Technique of immunoapheresis in heterotopic and orthotopic xenotransplantation of pig hearts into cynomolgus and rhesus monkeys

Transplantation proceedings, 2000-08, Vol.32 (5), p.1087-1088

2000

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Rupture of splenic artery aneurysm in a pregnant patient with portal hypertension

American journal of obstetrics and gynecology, 1996-05, Vol.174 (5), p.1665-1666

1996

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Die operative Therapie einer polytopen Wirbelsäulenmetastasierung bei malignem Phäochromocytom

Zeitschrift für orthopädie und ihre grenzgebiete, 1995, Vol.133 (2), p.176-179

1995

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Leiomyosarkom der Zunge

Laryngo- rhino- otologie, 1993-07, Vol.72 (7), p.342-345

1993

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Zur Differentialdiagnose gutartiger Mittelohrtumoren

Laryngo- rhino- otologie, 1994-07, Vol.73 (7), p.358-362

1994

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Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene

Journal of medical genetics, 2002-11, Vol.39 (11), p.812-816

2002

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IG-therasorb immunoapheresis in orthotopic xenotransplantation of baboons with landrace pig hearts

Transplantation, 2000-01, Vol.69 (2), p.208

2000

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Das kongenitale Fibrosesyndrom - Überlegungen zur Ätiologie, Genetik und chirurgischen Therapie

Klinische Monatsblätter für Augenheilkunde, 1990-08, Vol.197 (8), p.118-122

1990

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Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains

European journal of human genetics : EJHG, 2000-04, Vol.8 (4), p.280-285

2000

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The phenotypic spectrum of CADASIL: Clinical findings in 102 cases

Annals of neurology, 1998-11, Vol.44 (5), p.731-739

1998

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Spontaneous recovery of a childhood onset mitochondrial myopathy caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene

Journal of medical genetics, 2004-06, Vol.41 (6), p.e75-e75

2004

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Coenzyme Q10 deficiency and isolated myopathy

Neurology, 2006-01, Vol.66 (2), p.253-255

2006

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Oncocytic metaplasia/neoplasia--morphology, biochemistry, molecular genetics

Der Pathologe, 1998-02, Vol.19 (2), p.104-114

Müller-Höcker, J

1998

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Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited

Neuropathology and applied neurobiology, 2007-10, Vol.33 (5), p.544-559

2007

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Defects of the respiratory chain in the normal human liver and in cirrhosis during aging

Hepatology (Baltimore, Md.), 1997, Vol.26 (3), p.709-719

1997

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MesP1 drives vertebrate cardiovascular differentiation through Dkk-1-mediated blockade of Wnt-signalling

Chloroquine-induced phospholipidosis of the kidney mimicking fabry's disease: Case report and review of the literature

Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study

De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy

A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy

Renal Fanconi syndrome: first sign of partial respiratory chain complex IV deficiency

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene

Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies

Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts

Technique of immunoapheresis in heterotopic and orthotopic xenotransplantation of pig hearts into cynomolgus and rhesus monkeys

Rupture of splenic artery aneurysm in a pregnant patient with portal hypertension

Die operative Therapie einer polytopen Wirbelsäulenmetastasierung bei malignem Phäochromocytom

Leiomyosarkom der Zunge

Zur Differentialdiagnose gutartiger Mittelohrtumoren

Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene

IG-therasorb immunoapheresis in orthotopic xenotransplantation of baboons with landrace pig hearts

Das kongenitale Fibrosesyndrom - Überlegungen zur Ätiologie, Genetik und chirurgischen Therapie

Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains

The phenotypic spectrum of CADASIL: Clinical findings in 102 cases

Spontaneous recovery of a childhood onset mitochondrial myopathy caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene

Coenzyme Q10 deficiency and isolated myopathy

Oncocytic metaplasia/neoplasia--morphology, biochemistry, molecular genetics

Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited

Defects of the respiratory chain in the normal human liver and in cirrhosis during aging

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