Results 121 to 130 of about 5,912 (202)

Plasma proteome correlations with liver stiffness in pediatric cholestasis implicate epithelial to mesenchymal transition. [PDF]

Hepatol Commun
Shneider BL, Kanchi RS, Grimm SL, Devaraj S, Emamaullee J, Schraw J, Lupo PJ, Bezerra JA, Loomes KM, Magee JC, Sokol RJ, Wang KS, Kriegmeier A, Hsu E, Molleston JP, Rosenthal P, Kohli R, Karpen SJ, Horslen SP, Jensen MK, Barbetta A, Coarfa C, Childhood Liver Disease Research Network.   +22 more
europepmc   +1 more source

Case Report: α1-antitrypsin deficiency causing persistent pleural effusion and multilobar alveolar emphysema in a young dog. [PDF]

Front Vet Sci
Doulidis PG, Frizzo-Ramos C, Bertram CA, Grünzweil OM, Kneissl SM, Degasperi B, Hirt RA, Burgener IA, Luckschander-Zeller N.   +8 more
europepmc   +1 more source

Rare but relevant: Genetic liver disease in the general medical setting. [PDF]

Clin Med (Lond)
Allouni S, Ala A.
europepmc   +1 more source

Abdominal Lymphatic Malformations Presenting as Protein-Losing Enteropathy. [PDF]

ACG Case Rep J
Thomas J, Roma K, Bhat I.
europepmc   +1 more source

Alpha-1 antitrypsin in COVID-19 patients: a dual-center screening study in Malaysia. [PDF]

Ann Saudi Med
Musa N, Wan Azman WN, Nazri NAM, Tuan Ismail TS, Harun A, Yaacob NM, Sulong S, Sirajudeen KNS, Mat MC, Zulkeflee HA.   +9 more
europepmc   +1 more source

Functional and clinical significance of novel SERPINA1 variants on alpha-1 antitrypsin deficiency. [PDF]

Respir Res
Matamala N, Osaba L, Drobnic E, Gil-Martín S, Martín-Galiano AJ, Almadana-Pacheco V, Cazorla MJ, Costa F, Souza-Sokoloski C, Çörtük M, Serra-Fortuny M, Ortiz-de Saracho J, Lloret-Queraltó JA, Rodriguez-Lázaro N, Michel-de la Rosa FJ, Rodríguez-Hermosa JL, Saldaña-Pérez L, Akıncı E, Alonso J, Benítez-Buelga C, Gómez-Mariano G, López-Campos JL, Martínez-Delgado B.   +22 more
europepmc   +1 more source

L-ANTITRYPSIN DEFICIENCY. THE ALGORITHM OF ACTIONS IN MAKING A DIAGNOSIS AND DETERMINING THE TACTICS OF PATIENT MANAGEMENT

Медицина в Кузбассе
The article presents a clinical lecture on alpha-1-antitrypsin (A1AT) deficiency, a genetically determined disease caused by A1AT deficiency in blood serum and manifested in the form of chronic obstructive pulmonary disease, emphysema, liver and vascular
Надежда Григорьевна Ганюкова, Людмила Сергеевна Гофман, Марина Геннадьевна Якушенко, Светлана Ивановна Елгина, Елена Владимировна Рудаева, Кира Борисовна Мозес   +5 more
doaj  

Alpha1-Antitrypsin in Lung Diseases: A Cross-Sectional Observational Study. [PDF]

Int J Mol Sci
Páska C, Barta I, Csoma Z, Gajdócsi R, Szél V, Kerpel-Fronius A, Solymosi D, Örlős Z, Antus B.   +8 more
europepmc   +1 more source

Stereo-random oligonucleotides enable efficient recruitment of ADAR in vitro and in vivo. [PDF]

Nat Commun
Pfeiffer LS, Merkle T, Vogel P, Jarmoskaite I, Geisinger JM, Latifi N, Herrera-Barrera M, Zhang F, Groß L, Schlitz C, Hofacker DT, Lochmann C, Fumagalli D, Gackstatter S, Deisling V, Kay MA, Li JB, Stafforst T.   +17 more
europepmc   +1 more source

α1-Antitrypsin (AAT; A1AT; SERPINA1); histone deacetylase 7 (HDAC7) [PDF]

Science-Business eXchange, 2012
openaire   +1 more source