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References (2)

Title : Two new mutations in the CEL gene causing diabetes and hereditary pancreatitis: How to correctly identify MODY8 cases - El Jellas_2021_J.Clin.Endocrinol.Metab__
Author(s) : El Jellas K , Dusatkova P , Haldorsen IS , Molnes J , Tjora E , Johansson BB , Fjeld K , Johansson S , Pruhova S , Groop L , Lohr JM , Njolstad PR , Molven A
Ref : J Clinical Endocrinology Metab , : , 2021
Abstract : El Jellas_2021_J.Clin.Endocrinol.Metab__
ESTHER : El Jellas_2021_J.Clin.Endocrinol.Metab__
PubMedSearch : El Jellas_2021_J.Clin.Endocrinol.Metab__
PubMedID: 34850019
Gene_locus related to this paper: human-CEL

Title : Diagnostic algorithm for familial chylomicronemia syndrome - Stroes_2017_Atheroscler.Suppl_23_1
Author(s) : Stroes E , Moulin P , Parhofer KG , Rebours V , Lohr JM , Averna M
Ref : Atheroscler Suppl , 23 :1 , 2017
Abstract : Stroes_2017_Atheroscler.Suppl_23_1
ESTHER : Stroes_2017_Atheroscler.Suppl_23_1
PubMedSearch : Stroes_2017_Atheroscler.Suppl_23_1
PubMedID: 27998715