D020163DisordersC10.228.140.163.100.937.750C16.320.322.828C16.320.565.100.940.750C16.320.565.189.937.750C18.452.132.100.937.500C18.452.648.100.940.500C18.452.648.189.937.500340.997535Ornithine Carbamoyltransferase Deficiency Diseaseprns:emailEncryptedemail addressprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:mainImagephotoprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:meshTreeNumberMeSH tree numberprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:positionInDepartmentposition in departmentprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierDepartmentvivo:hrJobTitleHR job titleInformation ResourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson9686349Whitington PF, Alonso EM, Boyle JT, Molleston JP, Rosenthal P, Emond JC, Millis JMJournal of inherited metabolic diseaseLiver transplantation for the treatment of urea cycle disorders. J Inherit Metab Dis. 1998; 21 Suppl 1:112-8.J Inherit Metab Dis1998-01-01T00:00:001998Liver transplantation for the treatment of urea cycle disorders.Obstetrics & GynecologySurgery-General SurgeryPediatrics-Developmental and Behavioral3944708Batshaw ML, Msall M, Beaudet AL, Trojak JThe Journal of pediatricsRisk of serious illness in heterozygotes for ornithine transcarbamylase deficiency. J Pediatr. 1986 Feb; 108(2):236-41.J Pediatr1986-02-01T00:00:001986Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency.6717540Msall M, Batshaw ML, Suss R, Brusilow SW, Mellits EDThe New England journal of medicineNeurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies. N Engl J Med. 1984 Jun 07; 310(23):1500-5.N Engl J Med1984-06-07T00:00:001984Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.0.4196210.03350813research area of0.4206580.01583394subject area forUniversity of ChicagoJamesMillis3W9kAq0ZEP/5hHlsaUXv9Gq0+s+oJames Millis41.78927490000000-87.601250000000001299Millis, JamesProfessorDavidOuyangDavid Ouyang41.78927490000000-87.60125000000000245Ouyang, DavidClinical Associate ProfessorMichael E.MsallMichael E. Msall41.78927490000000-87.60125000000000314Msall, Michael E.Professortrue1Clinical Associate ProfessorClinical Associate Professortrue1ProfessorProfessortrue1ProfessorProfessor21956151Lipskind S, Loanzon S, Simi E, Ouyang DWJournal of perinatology : official journal of the California Perinatal AssociationHyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids. J Perinatol. 2011 Oct; 31(10):682-4.J Perinatol2011-10-01T00:00:002011Hyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids.