Literature DB >> 1430368

Annually recurring acroerythema and hereditary lactate dehydrogenase M-subunit deficiency.

G Nazzari1, F Crovato.   

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Year:  1992        PMID： 1430368     DOI： 10.1016/s0190-9622(08)80735-9

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN： 0190-9622            Impact factor:   11.527


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  3 in total

1.  Diagnostic evaluation of rhabdomyolysis.

Authors:  Jessica R Nance; Andrew L Mammen
Journal:  Muscle Nerve       Date:  2015-03-14       Impact factor: 3.217

2.  Hepatic Lactate Dehydrogenase A: An RNA Interference Target for the Treatment of All Known Types of Primary Hyperoxaluria.

Authors:  Gema Ariceta; Kelly Barrios; Bob D Brown; Bernd Hoppe; Ralf Rosskamp; Craig B Langman
Journal:  Kidney Int Rep       Date:  2021-02-03

3.  Annually Recurring Erythema Annulare Centrifugum: A New Case Series with Review of the Literature.

Authors:  Martina Maurelli; Paolo Gisondi; Chiara Colato; Giampiero Girolomoni
Journal:  Case Rep Dermatol       Date:  2021-06-10
  3 in total

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