Literature DB >> 7175018

Acute rhabdomyolysis with carnitine-palmityl-transferase deficiency.

P L Blanc, H Carrier, L Thomas, J M Chavaillon, D Robert.   

Abstract

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Year:  1982        PMID： 7175018     DOI： 10.1007/bf01716746

Source DB:  PubMed          Journal:  Intensive Care Med        ISSN： 0342-4642            Impact factor:   17.440


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  4 in total

1.  A disorder of muscle lipid metabolism and myoglobinuria. Absence of carnitine palmityl transferase.

Authors:  W J Bank; S DiMauro; E Bonilla; D M Capuzzi; L P Rowland
Journal:  N Engl J Med       Date:  1975-02-27       Impact factor: 91.245

2.  The mechanism of substrate inhibition of palmityl coenzyme A:carnitine palmityltransferase by palmityl coenzyme A.

Authors:  J Bremer; K R Norum
Journal:  J Biol Chem       Date:  1967-04-25       Impact factor: 5.157

3.  Disorders of lipid metabolism in muscle.

Authors:  S Di Mauro; C Trevisan; A Hays
Journal:  Muscle Nerve       Date:  1980 Sep-Oct       Impact factor: 3.217

4.  Carnitine palmityl transferase deficiency: myoglobinuria and respiratory failure.

Authors:  T Bertorini; Y Y Yeh; C Trevisan; E Stadlan; S Sabesin; S DiMauro
Journal:  Neurology       Date:  1980-03       Impact factor: 9.910
  4 in total
  2 in total

Review 1.  Muscle Carnitine Palmitoyltransferase II (CPT II) Deficiency: A Conceptual Approach.

Authors:  Pushpa Raj Joshi; Stephan Zierz
Journal:  Molecules       Date:  2020-04-13       Impact factor: 4.411

2.  Genetic test for Mendelian fatigue and muscle weakness syndromes.

Authors:  Aysha Karim Kiani; Bruno Amato; Silvia Maitz; Savina Nodari; Sabrina Benedetti; Francesca Agostini; Lorenzo Lorusso; Enrica Capelli; Astrit Dautaj; Matteo Bertelli
Journal:  Acta Biomed       Date:  2020-11-09
  2 in total

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