KimberlyAnnKrippsMD

PubMed

• Rubella virus-associated necrotizing granulomatous inflammation with extensive eyelid, ocular, and orbital involvement.
  Matthew A Pimentel, Donna H Kim, Lorne W Walker, Michelle B Noelck, Ludmila Perelygina, Kimberly A Kripps, Victoria W Cartwright, Tracy Funk, Sarah Green, Annie Kuo, J...> ;Pediatric Dermatology. 2023 May 18
• 7 citations
  Methionine Synthase Deficiency: Variable Clinical Presentation And Benefit Of Early Diagnosis And Treatment
  Kimberly A. Kripps, Leighann Sremba, Austin Larson, Johan L.K. Van Hove, Hoanh Nguyen, Erica L. Wright, David M. Mirsky, David Watkins, David S. Rosenblatt, David Kett...> ;Journal of Inherited Metabolic Disease. 2021 Oct 9
• 1 citations
  A Novel Intronic Pathogenic Variant in STAR With a Dominant Negative Mechanism Causes Attenuated Lipoid Congenital Adrenal Hyperplasia.
  Erin Finn, Kimberly A. Kripps, Christina D. Chambers, Michele Rapp, Naomi Meeks, Fang Xu, Wuyan Chen, Austin Larson, Natalie J. Nokoff> ;Journal of Investigative Medicine High Impact Case Reports. 2021 May 8
• 4 citations
  REVIEW: Practical strategies to maintain anabolism by intravenous nutritional management in children with inborn metabolic diseases.
  Kimberly A. Kripps, Peter R. Baker, Janet A. Thomas, Heather E. Skillman, Laurie Bernstein, Sommer Gaughan, Casey Burns, Curtis R. Coughlin, Shawn E. McCandless, Austi...> ;Molecular Genetics and Metabolism. 2021 May 7
• 2 citations
  A novel acceptor stem variant in mitochondrial tRNATyr impairs mitochondrial translation and is associated with a severe phenotype.
  Kimberly A. Kripps, Marisa W. Friederich, Ting Chen, Austin Larson, David M. Mirsky, Yue Wang, Kurenai Tanji, Kaz M. Knight, Lee-Jun C. Wong, Johan L.K. Van Hove> ;Molecular Genetics and Metabolism. 2020 Nov 24
• Unusual Neuroimaging in a Case of Rapidly Progressive Juvenile-Onset Krabbe Disease:
  Kimberly A. Kripps, Janell Kierstein, Daniel Nicklas, Julie Nelson, Michele L. Yang, Abigail Collins, Elizabeth Troy, Maria L. Escolar, John A Maloney, Ilana Neuberger...> ;Journal of Child Neurology. 2020 Jun 2
• 7 citations
  Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrum.
  Lisa Emrick, Jill A. Rosenfeld, Seema R. Lalani, Mahim Jain, Nilesh K. Desai, Austin Larson, Kimberly A. Kripps, Adeline Vanderver, Ryan J. Taft, Krista Bluske, Denise...> ;Genetics in Medicine. 2019 Jul 1
• Join now to see all