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Journal Abstract Search

204 related items for PubMed ID: 11595519

  • 1. Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiency.
    Kottlors M, Jaksch M, Ketelsen UP, Weiner S, Glocker FX, Lücking CH.
    Neuromuscul Disord; 2001 Nov; 11(8):757-9. PubMed ID: 11595519
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  • 2. Postinfectious Rhabdomyolysis in a 5-Year-Old Boy: When to Look a Little Deeper.
    Garoufi A, Vartzelis G, Kossiva L, Katsarou E, Soldatou A.
    Pediatr Emerg Care; 2015 Dec; 31(12):851-2. PubMed ID: 25513977
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  • 3. Adult-onset carnitine palmitoyl transferase II (CPT II) deficiency presenting with rhabdomyolysis and acute kidney injury.
    Akar HT, Yıldız Y, Mutluay R, Tekin E, Tokatlı A.
    CEN Case Rep; 2024 Apr; 13(2):81-85. PubMed ID: 37341884
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  • 4. Muscle Carnitine Palmitoyltransferase II (CPT II) Deficiency: A Conceptual Approach.
    Joshi PR, Zierz S.
    Molecules; 2020 Apr 13; 25(8):. PubMed ID: 32295037
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  • 5. Clinically symptomatic heterozygous carnitine palmitoyltransferase II (CPT II) deficiency.
    Joshi PR, Deschauer M, Zierz S.
    Wien Klin Wochenschr; 2012 Dec 13; 124(23-24):851-4. PubMed ID: 23184072
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  • 8. Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiency.
    Martín MA, Rubio JC, del Hoyo P, García A, Bustos F, Campos Y, Cabello A, Culebras JM, Arenas J.
    Hum Mutat; 2000 Jun 13; 15(6):579-80. PubMed ID: 10862092
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  • 13. Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: clinical, biochemical, and genetic features of adult-onset cases.
    Kilfoyle D, Hutchinson D, Potter H, George P.
    N Z Med J; 2005 Feb 25; 118(1210):U1320. PubMed ID: 15776096
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  • 15. Carnitine palmitoyltransferase II deficiency: molecular and biochemical analysis of 32 patients.
    Wieser T, Deschauer M, Olek K, Hermann T, Zierz S.
    Neurology; 2003 Apr 22; 60(8):1351-3. PubMed ID: 12707442
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  • 18. Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiency.
    Anichini A, Fanin M, Vianey-Saban C, Cassandrini D, Fiorillo C, Bruno C, Angelini C.
    Neurol Res; 2011 Jan 22; 33(1):24-32. PubMed ID: 20810031
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  • 19. Cause of recurrent rhabdomyolysis, carnitine palmitoyltransferase II deficiency and novel pathogenic mutation.
    Çakar NE, Gör Z, Yeşil G.
    Ideggyogy Sz; 2021 Mar 30; 74(3-4):135-138. PubMed ID: 33938664
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  • 20. Carnitine palmitoyltransferase-II deficiency: case presentation and review of the literature.
    Mccormick BJ, Chirila RM.
    Rom J Intern Med; 2021 Dec 01; 59(4):420-424. PubMed ID: 34118800
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