Results 121 to 130 of about 107,949,779 (166)

The Expanding Scope of Alpha 1 Antitrypsin Deficiency

Mayo Clinic Proceedings: Innovations, Quality & Outcomes
Friedrich Kueppers, MD
doaj   +1 more source

Alpha-1 antitrypsin deficiency in patients with chronic hepatitis

The Turkish Journal of Gastroenterology, 2012
Halis Şimşek, Aslı PINAR, Akif Altınbaş, Alparslan ALP, Yasemin H. BALABAN, Yahya BÜYÜKAŞIK, Osman ÖZCEBE, Gülşen HASÇELİK, Gökhan GEDİKOĞLU, Gonca Tatar   +9 more
doaj   +1 more source

Alpha-1-antitrypsin deficiency

, 2013
openaire   +1 more source

Alpha-1-antitrypsin deficiency

, 2018
openaire   +1 more source

Alpha-1 antitrypsin deficiency [PDF]

Respiratory Medicine, 2010
OBJECTIVE: To review the topic of alpha-1 antitrypsin (AAT) deficiency. METHOD: Narrative literature review. RESULTS: Much work has been carried out on this condition with many questions being answered but still further questions remain.
Noel G McElvaney, Tomás P. Carroll, Catherine M Greene   +2 more
exaly   +10 more sources

Alpha-1 antitrypsin deficiency–associated panniculitis

Journal of the American Academy of Dermatology, 2022
Background: Panniculitis represents a rare and potentially lethal manifestation of alpha-1 antitrypsin deficiency (AATD). Evidence regarding management is limited to case reports and small case series.
James Ralph, Noel G McElvaney, Tomás P. Carroll   +2 more
exaly   +2 more sources

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Alpha-1 Antitrypsin Deficiency

2023
Alpha-1 antitrypsin (AAT) deficiency is a common monogenic disorder in which there is a strong founder effect of a single missense mutation in SERPINA1, the gene encoding this major circulating serum anti-protease that is normally expressed primarily in hepatocytes.
Alisha M, Gruntman, Wen, Xue, Terence R, Flotte   +2 more
openaire   +3 more sources

Alpha-1 Antitrypsin Deficiency

Journal of Insurance Medicine, 2015
Alpha-1 antitrypsin deficiency is an inherited disorder that may cause severe lung and liver disease.
SK Kabra, Rakesh Lodha, Kana Jat
  +6 more sources

Alpha-1-antitrypsin augmentation therapy for alpha-1-antitrypsin deficiency

The American Journal of Medicine, 1988
Alpha-1-antitrypsin (A1AT) deficiency is a genetic disorder characterized by low serum levels of A1AT and a high risk for the development of emphysema. A1AT is the principal inhibitor of neutrophil elastase, such that a deficiency of A1AT results in insufficient anti-elastase protection in the lower respiratory tract, thus allowing neutrophil elastase ...
R C, Hubbard, R G, Crystal
openaire   +2 more sources

ALPHA‐1‐ANTITRYPSIN DEFICIENCY IN ADULTS

Acta Pathologica Japonica, 1986
A clinicopathological examination was carried out on eight adult patients with alpha‐1‐antitrypsin (ATT) deficiency. Phenotyping comfirmed five patients with PiMZ, two patients with PiZ‐, and one patient with PiZZ. Cirrhosis was found in six of the patients, four of whom had a history of excessive ethanol comsumption.
M, Kage, M, Kage, C T, Liew, Y, Xu, R L, Peters   +4 more
openaire   +2 more sources