H. Wick

Rapid differential diagnosis of carboxylase deficiencies and evaluation for biotin-responsiveness in a single blood sample

Terttu Suormala, H. Wick, Jean‐Pierre Bonjour et al. · Clinica Chimica Acta · 1985 · 90 citations

Single Blood Sample, Rapid Differential Diagnosis, Carboxylase Deficiencies +7

Biotinidase Deficiency: A Cause of Subacute Necrotizing Encephalomyelopathy (Leigh Syndrome). Report of a Case with Lethal Outcome

E. R. Baumgartner, Terttu Suormala, H. Wick et al. · Pediatric Research · 1989 · 82 citations · Full text

Inherited Metabolic Disease, Pathology, Lethal Outcome +7

Five Patients with a Biotin-Responsive Defect in Holocarboxylase Formation: Evaluation of Responsiveness to Biotin Therapy in Vivo and Comparative Biochemical Studies in Vi1

Terttu Suormala, Brian Fowler, Marinus Durán et al. · Pediatric Research · 1997 · 54 citations · Full text

Comparative Biochemical Studies, Biochemistry, Biotin Therapy +3

Analysis of glycogen storage disease by <i>in vivo</i>¹³C NMR comparison of normal volunteers with a patient

Nicolau Beckmann, Joachim Seelig, H. Wick · Magnetic Resonance in Medicine · 1990 · 50 citations

Late-onset holocarboxylase synthetase-deficiency: pre- and post-natal diagnosis and evaluation of effectiveness of antenatal biotin therapy

Terttu Suormala, Brian Fowler, C. Jakobs et al. · European Journal of Pediatrics · 1998 · 46 citations

Antenatal Biotin Therapy, Developmental Biology, Fertility +14