I. Paetzke

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

K. Gerbitz, D. Pongratz, T. Deufel, 1986, Klinische Wochenschrift.

Mitochondrial myopathy with diffuse activation and focal deficiency of mitochondrial ATPase and carnitine deficiency

D. Pongratz, J. Müller‐Höcker, G. Hübner, 1985, Virchows Archiv. B, Cell pathology including molecular pathology.

Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria

M. Durán, K. Gibson, T. Deufel, 1993, European Journal of Pediatrics.

Skeletal muscle sonography: a correlative study of echogenicity and morphology

D. Pongratz, C. Reimers, K Reimers, 1993, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies

T. Deufel, W. Endres, B. Kadenbach, 2005, Virchows Archiv A.

Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndrome

D. Zafeiriou, B. Koletzko, G. Kueffer, 1995, Brain and Development.

Therapy of complex I deficiency: Peripheral neuropathy during dichloroacetate therapy

H. Möller, G. Schuierer, H. Masur, 1995, European Journal of Pediatrics.

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.

D. Pongratz, K. Bise, B. Kadenbach, 1993, Archives of pathology & laboratory medicine.

Glycogenosis Type V (McArdle’s Disease) Mimicking Atypical Myositis

E. Neuen‐Jacob, G. Horneff, I. Paetzke, 2001, Clinical Rheumatology.

Type 2a fibre rhabdomyolysis in myoadenylate deaminase deficiency

D. Pongratz, C. Zimmer, G. Gosztonyi, 1991, Journal of Neurology.