Results 91 to 100 of about 22,986 (208)
From Ethanol to Salsolinol: Role of Ethanol Metabolites in the Effects of Ethanol [PDF]
, 2016 In spite of the global reputation of ethanol as the psychopharmacologically active ingredient of alcoholic drinks, the neurobiological basis of the central effects of ethanol still presents some dark sides due to a number of unanswered questions related ...
Acquas, E, Peana, At, Porru, S, Rosas, M
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Clinical, Cosmetic and Investigational DermatologyTanaporn Anuntrangsee, Kumutnart Chanprapaph, Wimolsiri Iamsumang Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, ThailandCorrespondence: Wimolsiri Iamsumang, Division of Dermatology,
Anuntrangsee T +2 more
doaj
Drug-induced dermatomyositis after lacosamide: A case report. [PDF]
, 2018 Here we describe a caseof a woman who had DM after treatment withlacosamide.
Gaffney, Rebecca G. +2 more
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Dysregulated Choline, Methionine, and Aromatic Amino Acid Metabolism in Patients with Wilson Disease: Exploratory Metabolomic Profiling and Implications for Hepatic and Neurologic Phenotypes. [PDF]
, 2019 Wilson disease (WD) is a genetic copper overload condition characterized by hepatic and neuropsychiatric symptoms with a not well-understood pathogenesis.
Czlonkowska, Anna +6 more
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Nicorandil-induced oral ulceration [PDF]
, 2008 Oral ulceration has many aetiological factors. The antianginal drug Nicorandil is becoming increasingly recognised as a causative factor for oral ulceration.
Ciantar, Marilou, Gibson, John
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Increased nociceptin/orphanin FQ plasma levels in hepatocellular carcinoma [PDF]
, 2004 AIM: The heptadecapeptide nociceptin alias orphanin FQ is the endogenous agonist of opioid receptor-like1 receptor. It is involved in modulation of pain and cognition.
Dunkel, Kinga +7 more
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The role of the pediatrican in the effort to prevent congenital malformations [PDF]
, 2011 N
Brent, Robert L, Dr.
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Nephrotic syndrome after treatment with D-penicillamine in a patient with Wilson’s disease
Romanian Journal of Laboratory Medicine, 2014 Wilson’s disease is an inherited autosomal recessive disorder of copper balance leading to accumulation of copper mainly in liver and brain result from absent or reduced function of copper-transporting P-type ATPase.
Kostadinova Anna D. +3 more
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, 2006 http://www.huveaux.fr/fr_santesite.aspWilson's disease is an autosomal recessive disorder of copper excess. This illness results from mutations of the ATP7B gene chromosome 13.
Chapuis, Philippe +4 more
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