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Pediatric Neurology|May 1, 1988
Rett syndrome: spinal cord neuropathologyA Oldfors, B Hagberg, H Nordgren, et al.
Brain & Development|January 1, 1990
The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte cultureJ Wahlström, I Witt-Engerström, L Mellquist, et al.
Diseases of the Colon and Rectum|February 1, 1984
Mandibular osteomas in familial polyposis coliS Bülow, J O Søndergaard, I Witt, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
A novel homozygous missense mutation (Val 325-->Ala) in the protein C gene causing neonatal purpura fulminansI Witt, S Beck, H H Seydewitz, et al.
Klinische Padiatrie|May 1, 1988
[131(I)-meta-iodobenzylguanidine treatment of 32 children with therapy-refractory neuroblastoma]F Berthold, U Feine, M Fischer, et al.
Endocrinology|August 1, 1981
Twenty-four-hour pattern of growth hormone secretion in the rhesus monkey: studies including alterations of the sleep/wake and sleep stage cyclesH J Quabbe, M Gregor, C Bumke-Vogt, et al.
The Journal of Biological Chemistry|December 25, 1979
Primary structure of yeast proteinase B inhibitor 2K Maier, H Müller, R Tesch, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1995
Rapid identification of gene defects in protein C deficiency by temperature gradient gel electrophoresisA Hernández, M Uhrberg, J Enczmann, et al.
Clinical Genetics|March 1, 1990
CSF and urine biogenic amine metabolites in Rett syndromeA Lekman, I Witt-Engerström, B Holmberg, et al.
Biochimica Et Biophysica Acta|November 29, 1985
Characterisation of calmodulin from Drosophila headsM Görlach, P Dieter, H H Seydewitz, et al.
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