Results 71 to 80 of about 1,216,936 (163)

PSYNDEX Tests Review für MBI-G - MASLACH BURNOUT INVENTORY - DEUTSCHE FASSUNG (BARTH, 1990)

, 1990
This is a PSYNDEX Tests Review of MBI-G - MASLACH BURNOUT INVENTORY - DEUTSCHE FASSUNG (BARTH, 1990). PSYNDEX Tests Reviews are written in German and describe and evaluate psychological and educational tests used in the German-speaking countries. PSYNDEX
Barth, Anne-Rose
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Early adversity and the comorbidity between metabolic disease and psychopathology

The Journal of Physiology, Volume 604, Issue 11, Page 4338-4377, 1 June 2026.
Abstract figure legend Hierarchical diagram representing the interplay between the genetic background and early life adversities and its effect on multiple physiological processes that ultimately impact on the risk for the comorbdity between psychopathology and cardiometabolic disorders.
Ameyalli Gómez‐Ilescas, Patricia Pelufo Silveira   +1 more
wiley   +1 more source

Philoikos zur Beförderung häuslicher Tugend und Glückseligkeit

Autopsie nach Exemplar der ULB Sachsen-AnhaltVorlageform des Erscheinungsvermerks: Leipzig, bei Johann Ambrosius Barth ...
Pischon, Johann Karl
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AAV9-TAZ Gene Replacement Ameliorates Cardiac TMT Proteomic Profiles in a Mouse Model of Barth Syndrome

Molecular Therapy: Methods & Clinical Development, 2019
Barth syndrome (BTHS) is a rare mitochondrial disease that causes severe cardiomyopathy and has no disease-modifying therapy. It is caused by recessive mutations in the gene tafazzin (TAZ), which encodes tafazzin—an acyltransferase that remodels the ...
Silveli Suzuki-Hatano, Madhurima Saha, Meghan S. Soustek, Peter B. Kang, Barry J. Byrne, W. Todd Cade, Christina A. Pacak   +6 more
doaj   +1 more source

A novel intronic splice site tafazzin gene mutation detected prenatally in a family with Barth syndrome

Balkan Journal of Medical Genetics, 2016
Barth syndrome (BTHS) is a rare X-linked disease characterized by dilated cardiomyopathy, proximal skeletal myopathy and cyclic neutropenia. It is caused by various mutations in the tafazzin (TAZ) gene located on Xq28 that results in remodeling of ...
Bakšienė M, Benušienė E, Morkūnienė A, Ambrozaitytė L, Utkus A, Kučinskas V   +5 more
doaj   +1 more source

Johann August Ehrlichs Chirurgische, auf Reisen, vorzüglich in den Hospitälern zu London gemachte Beobachtungen : nebst Angabe verbesserter Operationsarten und Abbildung neuer Instrumente

Vorlageform des Erscheinungsvermerks: Leipzig, bey Johann Ambrosius Barth. 1795.Ill. (Kupferst.
Ehrlich, Johann August
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Emerging roles of pyruvate dehydrogenase phosphatase 1: a key player in metabolic health

Frontiers in Physiology
Pyruvate dehydrogenase phosphatase (PDP), a structurally conserved member of the protein phosphatase C family (PP2C) of proteins, is a key regulatory enzyme responsible for reactivation of the mitochondrial gate-keeper, pyruvate dehydrogenase (PDH ...
Vikalp Kumar, Miriam L. Greenberg
doaj   +1 more source

Vorwort in Hans Barth "Osteria. Ein kulturgeschichtlicher Führer durch Italiens Osterien und Schenken vom Gardasee bis Capri.

, 2015
Guida delle osterie italiane (seconda ed. 1911), scritta da Hans Barth, corrispondente del Berliner Tageblatt a Roma dal 1886-1927. Si tratta di una descrizione umoristica delle osterie italiane, viste con l'occhio del viaggiatore tedesco che coglie l ...
Barth, Hans, OSWALD, Stephan Maria
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Chirurgische Beobachtungen : nebst hinzugefügter Beschreibung der in England gebräuchlichen Charpiemaschine

Vorlageform des Erscheinungsvermerks: Leipzig, bey Johann Ambrosius Barth. 1815.3 Ill.
Ehrlich, Johann August
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Barth syndrome : a mutational analysis of the BTHS gene [PDF]

, 1999
Barth syndrome is an X-linked recessive disorder affecting only males. The clinical features of Barth syndrome include cardiomyopathy, endocardial fibroelastosis, neutropenia, hypocholesterolemia, growth retardation, short stature and cyclic acidurias ...
Elliot, Ann M.
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