H. Wick - Concepedia

Author

H. Wick

University Children’s Hospital Basel

Also Known As

H WICK, H Wick, H. Wick, HUGO WICK, Hugo Wick

Publications

912

Citations

H-Index

Concepts

All Affiliations

University Children’s Hospital Basel Roche (Switzerland)University of Basel Boston Children's Hospital Cnopf´sche Kinderklinik

About

H. Wick is an author at University Children’s Hospital Basel specializing in medicine, metabolism, and health sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	17	548
2	Health Sciences	7	7	156
3	Biochemistry	6	6	228
4	Public Health	1	1	46
5	Biomolecular Engineering	1	1	54

H. Wick

Publications

847

Citations

H-Index

Page 1

	Year	Citations
Rapid differential diagnosis of carboxylase deficiencies and evaluation for biotin-responsiveness in a single blood sample Terttu Suormala, H. Wick, Jean‐Pierre Bonjour, Clinica Chimica Acta Single Blood SampleRapid Differential DiagnosisCarboxylase DeficienciesBiochemistryMedicine	1985	90
Biotinidase Deficiency: A Cause of Subacute Necrotizing Encephalomyelopathy (Leigh Syndrome). Report of a Case with Lethal Outcome E. R. Baumgartner, Terttu Suormala, H. Wick, Pediatric Research Inherited Metabolic DiseasePathologyLethal OutcomeDegenerative DiseaseNeurology	1989	82
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, Pediatric Research Comparative Biochemical StudiesBiochemistryBiotin TherapyPharmacologyBiotin-responsive Defect	1997	54
Analysis of glycogen storage disease by <i>in vivo</i><sup>13</sup>C NMR comparison of normal volunteers with a patient Nicolau Beckmann, Joachim Seelig, H. Wick Magnetic Resonance in Medicine	1990	50
Late-onset holocarboxylase synthetase-deficiency: pre- and post-natal diagnosis and evaluation of effectiveness of antenatal biotin therapy Terttu Suormala, Brian Fowler, C. Jakobs, European Journal of Pediatrics Antenatal Biotin TherapyDevelopmental BiologyFertilityPost-natal DiagnosisLate-onset Holocarboxylase Synthetase-deficiency	1998	46
Thiamine dependency in a patient with congenital lacticacidaemia due to pyruvate dehydrogenase deficiency H. Wick, Katrin Schweizer, R. Baumgartner Inflammation Research Congenital LacticacidaemiaPediatricsThiamine DependencyMetabolismDehydrogenase Deficiency	1977	42
Biotinidase Deficiency Associated with Renal Loss of Biocytin and Biotin E. R. Baumgartner, Terttu Suormala, H. Wick, Annals of the New York Academy of Sciences Biotin RequirementUrologyRenal FunctionMedicineBiotinidase Deficiency Associated	1985	39
Variants of citrullinaemia. H. Wick, C. Bachmann, R. Baumgartner, Archives of Disease in Childhood	1973	39
Comparison of patients with complete and partial biotinidase deficiency: Biochemical studies Terttu Suormala, E. R. Baumgartner, H. Wick, Journal of Inherited Metabolic Disease	1989	37
Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology. E. R. Baumgartner, H. Wick, Robert Maurer, PubMed NutritionElectrolyte DisorderHeart FailureRenal FunctionHematology	1979	37

Page 1