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Journal of Applied Clinical Medical Physics|January 20, 2006
Interobserver variation in cervical cancer tumor delineation for image-based radiotherapy planning among and within different specialtiesDee H Wu, Nina A Mayr, Yasemin Karatas, et al.
American Journal of Human Genetics|February 3, 2007
Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylationJohannes A Mayr, Olaf Merkel, Sepp D Kohlwein, et al.
AJNR. American Journal of Neuroradiology|June 1, 1994
Phase III multicenter trial of high-dose gadoteridol in MR evaluation of brain metastasesW T Yuh, D J Fisher, V M Runge, et al.
Clinical Case Reports|March 23, 2019
Mitochondrial complex deficiency by novel compound heterozygous <i>TMEM70</i> variants and correlation with developmental delay, undescended testicle, and left ventricular noncompaction in a Japanese patient: A case reportKeiichi Hirono, Fukiko Ichida, Natsuhito Nishio, et al.
JIMD Reports|February 23, 2013
MNGIE Syndrome: Liver Cirrhosis Should Be Ruled Out Prior to Bone Marrow TransplantationArmin Finkenstedt, Melanie Schranz, Sylvia Bösch, et al.
AJR. American Journal of Roentgenology|February 1, 1994
Brain parenchymal infection in bone marrow transplantation patients: CT and MR findingsW T Yuh, H D Nguyen, F Gao, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 10, 2025
Mitochondrial disorder diagnosis and management- what the pediatric neurologist wants to knowOliver Heath, René G Feichtinger, Melanie T Achleitner, et al.
Future Oncology (London, England)|September 17, 2011
Stereotactic body radiation therapy for prostate cancerHiromichi Ishiyama, Bin S Teh, Simon S Lo, et al.
Cancer|January 7, 2010
Ultra-early predictive assay for treatment failure using functional magnetic resonance imaging and clinical prognostic parameters in cervical cancerNina A Mayr, William T C Yuh, David Jajoura, et al.
Neuropediatrics|August 17, 2018
HTRA2 Defect: A Recognizable Inborn Error of Metabolism with 3-Methylglutaconic Aciduria as Discriminating Feature Characterized by Neonatal Movement Disorder and Epilepsy-Report of 11 PatientsReka Kovacs-Nagy, Gilles Morin, Maria Al Nouri, et al.
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