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Showing results for case venable
Your search for Casie Venable retrieved no results
Low-pressure Hydrocephalus in Children: A Case Series and Review of the Literature.
Smalley ZS, Venable GT, Einhaus S, Klimo P Jr. Smalley ZS, et al. Neurosurgery. 2017 Mar 1;80(3):439-447. doi: 10.1093/neuros/nyw046. Neurosurgery. 2017. PMID: 28362957 Review.
METHODS: Patients with LPH were identified from several sources, including institutional procedural databases and personal case logs. Electronic medical records were reviewed to collect demographic, clinical, surgical, and radiographic data to determine the presence of LPH …
METHODS: Patients with LPH were identified from several sources, including institutional procedural databases and personal case logs. …
Pseudoexstrophy.
Mitchell W, Venable D, Patel AJ. Mitchell W, et al. Urology. 1993 Feb;41(2):134-6. doi: 10.1016/0090-4295(93)90164-6. Urology. 1993. PMID: 8497983 Review.
Pseudoexstrophy is a rare, mild exstrophy variant which involves the major musculoskeletal defects of the exstrophy complex without any associated defect in the urinary system. A case is reported presenting at birth as an umbilical positional anomaly. ...
Pseudoexstrophy is a rare, mild exstrophy variant which involves the major musculoskeletal defects of the exstrophy complex without any asso …
COL1A1 and COL1A2 variants in Ehlers-Danlos syndrome phenotypes and COL1-related overlap disorder.
Venable E, Knight DRT, Thoreson EK, Baudhuin LM. Venable E, et al. Am J Med Genet C Semin Med Genet. 2023 Jun;193(2):147-159. doi: 10.1002/ajmg.c.32038. Epub 2023 Mar 9. Am J Med Genet C Semin Med Genet. 2023. PMID: 36896471
On the other hand, 9/10 potential OIEDS2 cases have a predominant EDS phenotype, including four with an initial diagnosis of hypermobile EDS (hEDS). An additional case with a predominant EDS phenotype had a COL1A1 arginine-to-cysteine variant that was originally misclassif …
On the other hand, 9/10 potential OIEDS2 cases have a predominant EDS phenotype, including four with an initial diagnosis of hypermobile EDS …
Empty sella syndrome.
Venable HP. Venable HP. J Natl Med Assoc. 1977 Apr 1;69(4):243-7. J Natl Med Assoc. 1977. PMID: 853537 Free PMC article.
An attempt is made to determine why these syndromes may coexist. A detailed case report is presented which emphasizes the definitive signs and symptoms that are found in patients having both of these syndromes, and differentiation is made between idiopathic and secondary E …
An attempt is made to determine why these syndromes may coexist. A detailed case report is presented which emphasizes the definitive …
A rare case of a clinically significant anti-M alloantibody in a heart transplant recipient.
Sharma D, Johnson M, Venable J, Eichbaum Q, Stiefel E. Sharma D, et al. Transfus Apher Sci. 2022 Feb;61(1):103284. doi: 10.1016/j.transci.2021.103284. Epub 2021 Sep 24. Transfus Apher Sci. 2022. PMID: 34865973
Rarely, these antibodies have been reported to react at physiologic temperatures, resulting in clinically significant hemolytic transfusion reactions or hemolytic disease of the fetus and newborn. PATIENT AND METHODS: We describe a case of an acute hemolytic transfusion re …
Rarely, these antibodies have been reported to react at physiologic temperatures, resulting in clinically significant hemolytic transfusion …
A TRIP11:: FLT3 gene fusion in a patient with myeloid/lymphoid neoplasm with eosinophilia and tyrosine kinase gene fusions: a case report and review of the literature.
Venable ER, Gagnon MF, Pitel BA, Palmer JM, Peterson JF, Baughn LB, Hoppman NL, Greipp PT, Ketterling RP, Patnaik MS, Kelemen K, Xu X. Venable ER, et al. Cold Spring Harb Mol Case Stud. 2023 Mar 24;9(1):a006243. doi: 10.1101/mcs.a006243. Print 2023 Feb. Cold Spring Harb Mol Case Stud. 2023. PMID: 36627146 Free PMC article. Review.
A diagnosis of MLN-TK was rendered. To the best of our knowledge, we report the third case of MLN-TK with a TRIP11::FLT3 gene fusion. In contrast to previously described cases, our case exhibited distinctly mild clinical features and disease behavior, emphasizing th …
A diagnosis of MLN-TK was rendered. To the best of our knowledge, we report the third case of MLN-TK with a TRIP11::FLT3 gene fusion. …
Disseminated Nocardia in an Immunocompetent Host.
Wintheiser GA, Venable ER, Temesgen Z. Wintheiser GA, et al. Mayo Clin Proc. 2021 Apr;96(4):847-848. doi: 10.1016/j.mayocp.2020.11.019. Mayo Clin Proc. 2021. PMID: 33814090 No abstract available.
Nodular Sclerosing Hodgkin Lymphoma With Paraneoplastic Cerebellar Degeneration.
Teh LD, Culp LH, Venable A. Teh LD, et al. Fed Pract. 2022 Aug;39(Suppl 3):S18-S19. doi: 10.12788/fp.0293. Epub 2022 Jul 14. Fed Pract. 2022. PMID: 36426105 Free PMC article.
Most of these autoimmune phenomena involve older adult patients with abrupt, acute presentations. CASE PRESENTATION: We report an atypical case of a young adult female patient with slow progressive onset of PCD symptoms with subsequent detection and treatment of Hod …
Most of these autoimmune phenomena involve older adult patients with abrupt, acute presentations. CASE PRESENTATION: We report an aty …
Fournier's gangrene in children.
Adams JR Jr, Mata JA, Venable DD, Culkin DJ, Bocchini JA Jr. Adams JR Jr, et al. Urology. 1990 May;35(5):439-41. doi: 10.1016/0090-4295(90)80088-5. Urology. 1990. PMID: 2186554 Review.
Necrotizing fasciitis of the genitalia is a rare urologic emergency that is especially uncommon in children. We report a case of Fournier's gangrene in a four-year-old boy and analyze the data from 55 previously reported cases. ...
Necrotizing fasciitis of the genitalia is a rare urologic emergency that is especially uncommon in children. We report a case of Four …
82 results