S. Kulakowski

Reduced TrkB expression results in precocious age-like changes in neuromuscular structure, neurotransmission, and muscle function.

K. Personius, Sara D. Parker, S. Kulakowski, 2011, Journal of applied physiology.

Congenital muscular dystrophy and cerebral CT scan anomalies Results of a collaborative study of the Société de Neurologie Infantile

J. R. Moore, B. Echenne, O. Dulac, 1986, Journal of the Neurological Sciences.

Purine metabolism in Duchenne muscular dystrophy.

C. V. van Bennekom, C. De Bruyn, M. Müller, 1980, Advances in experimental medicine and biology.

Metabolite profiling of human muscle extracts by isotachophoresis

F. Oerlemans, C. V. Bennekom, S. Kulakowski, 1981, Journal of Inherited Metabolic Disease.

Enzymes of purine metabolism in muscle specimens from patients with Duchenne-type muscular dystrophy.

F. Oerlemans, C. V. van Bennekom, C. De Bruyn, 1984, Advances in experimental medicine and biology.

Differential responses to mitogen stimulation in lymphocytes from normal individuals and Lesch-Nyhan patients: influence of the bicarbonate buffer system.

E. Vámos, G. Delespesse, J. Duchateau, 1980, Clinical and Experimental Immunology.

Severe congenital cutis laxa with pulmonary emphysema: a family with three affected sibs.

I. Liebaers, G. Vandevelde, L. Van Maldergem, 1988, American journal of medical genetics.

Reduced TrkB expression results in precocious age-like changes in neuromuscular structure, neurotransmission, and muscle function.

K. Personius, Sara D. Parker, S. Kulakowski, 2011, Journal of applied physiology.