language:
Find link is a tool written by Edward Betts.Alpha 1-antitrypsin is a redirect to Alpha-1 antitrypsin
searching for Alpha 1-antitrypsin 67 found (125 total)
alternate case: alpha 1-antitrypsin
Panniculitis
(1,183 words)
[view diff]
exact match in snippet
view article
find links to article
sarcoidosis with cutaneous involvement (seen in up to 20 percent); Alpha 1-antitrypsin deficiency Crohn's disease This is not a complete list of possiblePAS diastase stain (296 words) [view diff] no match in snippet view article find links to article
is also used to identify alpha-1 antitrypsin globules in hepatocytes, which is a characteristic finding of alpha-1 antitrypsin deficiency. PAS diastaseEmphysema (4,353 words) [view diff] no match in snippet view article find links to article
develop with the effects of tobacco smoking, and other risk factors. Alpha-1 antitrypsin deficiency is a genetic risk factor that may lead to the conditionAugmentation (pharmacology) (316 words) [view diff] exact match in snippet view article
L-DOPA outside the brain. To give α1 antitrypsin to someone with alpha 1-antitrypsin deficiency. Wright, BM; Eiland EH, 3rd; Lorenz, R (March 2013). "AugmentationKamada (company) (678 words) [view diff] exact match in snippet view article
approved by the FDA to treat alpha 1-antitrypsin deficiency. The active ingredient in the drug is the protein alpha-1 antitrypsin, for patients with a geneticNeonatal cholestasis (1,364 words) [view diff] no match in snippet view article find links to article
cholestasis caused by alpha-1 antitrypsin deficiency does not have any specific treatment. Instead, children with alpha-1 antitrypsin deficiency are primarilyChildren's Liver Disease Foundation (303 words) [view diff] exact match in snippet view article find links to article
on the main liver diseases affecting children (biliary atresia, alpha 1-antitrypsin deficiency, autoimmune hepatitis, hepatitis A, hepatitis B, hepatitisList of MeSH codes (C17) (3,128 words) [view diff] no match in snippet view article
The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM)List of genes mutated in cutaneous conditions (108 words) [view diff] exact match in snippet view article find links to article
MEN2A, MEN2B SAMD9 Familial tumoral calcinosis SERPINA1 Alpha 1-antitrypsin Alpha-1 antitrypsin deficiency panniculitis SLC39A4 Acrodermatitis enteropathicaMAATS1 (420 words) [view diff] no match in snippet view article find links to article
Gardiner-Garden M (Oct 2003). "Are polymorphic markers within the alpha-1-antitrypsin gene associated with risk of human immunodeficiency virus diseaseIntellia Therapeutics (1,607 words) [view diff] no match in snippet view article find links to article
candidates with potential applications in diseases including cancer, alpha-1 antitrypsin deficiency, and hemophilia. The company is also working on a varietyArrowhead Pharmaceuticals (340 words) [view diff] exact match in snippet view article find links to article
focuses on treatments for hepatitis B, liver disease associated with alpha 1-antitrypsin deficiency and cardiovascular disease. The company has sixteen productsFocal lung pneumatosis (780 words) [view diff] exact match in snippet view article find links to article
sometimes be involved. Other conditions associated with lung bullae are: Alpha 1-antitrypsin deficiency Marfan syndrome Ehlers–Danlos syndromes Cocaine smokingBronchiectasis (6,716 words) [view diff] exact match in snippet view article find links to article
and recurrent lower respiratory tract infections. Individuals with alpha 1-antitrypsin deficiency have been found to be particularly susceptible to bronchiectasisLiver disease (2,820 words) [view diff] exact match in snippet view article find links to article
and Wilson's disease. Liver damage is also a clinical feature of alpha 1-antitrypsin deficiency and glycogen storage disease type II. In transthyretin-relatedDick Campbell (singer-songwriter) (1,056 words) [view diff] no match in snippet view article
had Alpha-1 antitrypsin deficiency; an inherited genetic disorder, which leads to lung damage due to the lack of the protective protein, Alpha-1 antitrypsinHepatocellular carcinoma (9,623 words) [view diff] exact match in snippet view article find links to article
pyrrolizidine alkaloids. Certain diseases, such as hemochromatosis and alpha 1-antitrypsin deficiency, markedly increase the risk of developing HCC. MetabolicProgressive disease (388 words) [view diff] no match in snippet view article find links to article
retinal detachment is rapidly progressive. Lungs: Emphysema due to alpha-1 antitrypsin deficiency is a slowly progressive pulmonary disease. Kidneys: Goodpasture'sSimple Explanation (889 words) [view diff] exact match in snippet view article find links to article
spleen ruptures in the middle of it. House thinks she could have Alpha 1-antitrypsin deficiency, so Thirteen and Taub run her AAT proteins. Foreman takesWeber–Christian disease (198 words) [view diff] no match in snippet view article find links to article
is named after Frederick Parkes Weber and Henry Asbury Christian. Alpha-1 antitrypsin deficiency panniculitis List of cutaneous conditions Rapini, RonaldNeonatal jaundice (3,247 words) [view diff] exact match in snippet view article find links to article
intrahepatic cholestasis, bile duct paucity, Alagille syndrome, alpha 1-antitrypsin deficiency, and other pediatric liver diseases should be consideredHealth of Frédéric Chopin (1,705 words) [view diff] exact match in snippet view article find links to article
infertility, which favours the cystic fibrosis hypothesis. A hypothesis of alpha 1-antitrypsin deficiency was proposed by Kuzemko in 1994. Mitral stenosis was aVariegate porphyria (1,020 words) [view diff] no match in snippet view article find links to article
(July 1988). "Linkage between the variegate porphyria (VP) and the alpha-1-antitrypsin (PI) genes on human chromosome 14". Hum. Genet. 79 (3): 289–90. doi:10Hepatitis (16,797 words) [view diff] no match in snippet view article find links to article
causes of hepatitis include alpha-1-antitrypsin deficiency, hemochromatosis, and Wilson's disease. In alpha-1-antitrypsin deficiency, a co-dominant mutationBrooke McCarter (667 words) [view diff] no match in snippet view article find links to article
December 22, 2015, at the age of 52 from the genetic liver disorder Alpha-1 antitrypsin deficiency (A1AD). His death increased awareness of this rare disorderVanishing bile duct syndrome (272 words) [view diff] no match in snippet view article find links to article
disease Von Meyenburg complex Trisomy 17, 18 and 21 Cystic fibrosis Alpha 1 antitrypsin deficiency Trihydroxycoprostanic acidemia Byler's disease Bile ductMaryAnn Lippert (420 words) [view diff] no match in snippet view article find links to article
suffering from chronic obstructive pulmonary disease, caused by Alpha-1 Antitrypsin Deficiency [1]. She was succeeded by Vruwink. After leaving the AssemblyFatty liver disease (3,896 words) [view diff] exact match in snippet view article find links to article
inflammatory bowel disease, HIV, hepatitis C (especially genotype 3), and alpha 1-antitrypsin deficiency The fatty change represents the intracytoplasmatic accumulationObstructive lung disease (1,279 words) [view diff] exact match in snippet view article find links to article
transplantation is also performed for severe COPD in carefully chosen cases. Alpha 1-antitrypsin deficiency is a fairly rare genetic condition that results in COPDChromosome 14 (1,831 words) [view diff] no match in snippet view article find links to article
following diseases are some of those related to genes on chromosome 14: Alpha-1 antitrypsin deficiency Alzheimer disease Burkitt's lymphoma (t8;14) congenitalMystery Diagnosis (603 words) [view diff] exact match in snippet view article find links to article
disorders, well-known conditions such as epilepsy, Myasthenia gravis, Alpha 1-antitrypsin deficiency, heart disease, Crohn's disease, pulmonary hypertensionRaymond L. Rodriguez (3,788 words) [view diff] no match in snippet view article find links to article
Rodriguez, R.L. and Katoh, S. 1999. Production of functional human alpha-1-antitrypsin in plant cell culture. Applied Microbial Biotechnology. 52:516-516CDIPT (538 words) [view diff] no match in snippet view article find links to article
PMID 15489334. de Serres FJ, Luisetti M, Ferrarotti I, et al. (2005). "Alpha-1 antitrypsin deficiency in Italy: regional differences of the PIS and PIZ deficiencyNontuberculous mycobacteria (1,691 words) [view diff] exact match in snippet view article find links to article
bronchiectasis, and prior tuberculosis. It is not uncommon for alpha 1-antitrypsin deficiency, Marfan syndrome, and primary ciliary dyskinesia patientsHNF1B (1,254 words) [view diff] no match in snippet view article find links to article
Perlmutter DH (2002). "Cell-specific involvement of HNF-1beta in alpha(1)-antitrypsin gene expression in human respiratory epithelial cells". Am. J. PhysiolPulmonology (2,111 words) [view diff] exact match in snippet view article find links to article
focusing on: hereditary diseases affecting the lungs (cystic fibrosis, alpha 1-antitrypsin deficiency) exposure to toxicants (tobacco smoke, asbestos, exhaustAMFR (1,117 words) [view diff] no match in snippet view article find links to article
increases solubility and facilitates degradation of the Z variant of alpha-1-antitrypsin". Biochem. Biophys. Res. Commun. 349 (4): 1285–93. doi:10.1016/jElastic fiber (1,420 words) [view diff] no match in snippet view article find links to article
have been directly associated with alterations in the elastin gene. Alpha-1 antitrypsin deficiency is a genetic disorder where elastin is excessively degradedFOXA2 (1,550 words) [view diff] exact match in snippet view article find links to article
nuclear factors function in the regulation of transthyretin and alpha 1-antitrypsin genes". Molecular and Cellular Biology. 9 (4): 1415–25. doi:10.1128/mcbJohn Cipollina (1,277 words) [view diff] no match in snippet view article find links to article
Cipollina died on May 29, 1989, at age 45. His cause of death was alpha-1 antitrypsin deficiency, which he suffered from most of his life and which isVertex Pharmaceuticals (3,315 words) [view diff] no match in snippet view article find links to article
sickle cell disease, beta thalassemia, Duchenne muscular dystrophy, alpha-1 antitrypsin deficiency, pain, and APOL1-mediated kidney diseases. In 2014, VertexList of diseases (A) (1,929 words) [view diff] exact match in snippet view article
universalis Alopecia universalis onychodystrophy vitiligo Alpers disease Alpha 1-antitrypsin deficiency Alpha-2 deficient collagen disease Alpha-ketoglutarateGranulomatous mastitis (2,026 words) [view diff] exact match in snippet view article find links to article
hyperprolactinemia with additional triggers such as local trauma or irritation. Alpha 1-antitrypsin deficiency was documented in one case and interferon-alpha therapyList of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (1,399 words) [view diff] exact match in snippet view article find links to article
Sanfilippo syndrome 277.6 Other deficiencies of circulating enzymes Alpha 1-antitrypsin deficiency Biotinidase deficiency Hereditary angioedema 277.7 DysmetabolicHNF1A (2,738 words) [view diff] exact match in snippet view article find links to article
"Interaction of a liver-specific nuclear factor with the fibrinogen and alpha 1-antitrypsin promoters". Science. 238 (4827): 688–92. Bibcode:1987Sci...238..688CList of genetic disorders (969 words) [view diff] exact match in snippet view article find links to article
18p D 1:50,000 21-hydroxylase deficiency 6p21.3 recessive 1:15,000 Alpha 1-antitrypsin deficiency 14q32 co-dominant, 1:2,500-5,000 AAA syndromeDara Kass (1,255 words) [view diff] no match in snippet view article find links to article
youngest son, Sammy, was diagnosed with a rare condition known as alpha-1 antitrypsin deficiency, which results in severely impaired liver function. WhileRikard Wolff (1,756 words) [view diff] no match in snippet view article find links to article
suffered from pulmonary emphysema since 1988 due to the genetic disease alpha-1 antitrypsin deficiency and died on 17 November 2017, aged 59. 1980: Sverige åtBiliary atresia (2,730 words) [view diff] no match in snippet view article find links to article
differential diagnoses are extensive and include: Alagille syndrome, alpha-1-antitrypsin deficiency, Byler disease (progressive familial intrahepatic cholestasis)Port (medical) (3,085 words) [view diff] exact match in snippet view article
Delivering medications to patients with immune disorders. For treating alpha 1-antitrypsin deficiency with replacement therapy For delivering radiopaque contrastLung transplantation (4,282 words) [view diff] exact match in snippet view article find links to article
idiopathic (formerly known as "primary") pulmonary hypertension; 5% alpha 1-antitrypsin deficiency; 2% replacing previously transplanted lungs that haveJaundice (5,113 words) [view diff] exact match in snippet view article find links to article
deficiency Pyruvate kinase deficiency ABO/Rh blood type autoantibodies Alpha 1-antitrypsin deficiency Alagille syndrome (genetic defect resulting in hypoplasticQuicksilver Messenger Service (3,888 words) [view diff] exact match in snippet view article find links to article
at the age of 45 from complications of emphysema exacerbated by Alpha 1-antitrypsin deficiency. Some of Cipollina's equipment is displayed at the RockKeith Pollard (rugby league) (785 words) [view diff] exact match in snippet view article
Road Lad" during December 2018, the net proceeds of which go to the Alpha 1-antitrypsin deficiency (A1AD) charity; Alpha-1 UK Support Group, his son JasonLiver cancer (6,092 words) [view diff] no match in snippet view article find links to article
development. Genetic conditions: untreated hereditary hemochromatosis, alpha-1-antitrypsin deficiency, glycogen storage diseases, porphyria cutanea tarda, Wilson's23andMe (6,260 words) [view diff] no match in snippet view article find links to article
Parkinson's disease, celiac disease, hereditary thrombophilia, alpha-1 antitrypsin deficiency, glucose-6-phosphate dehydrogenase deficiency, early-onsetPneumothorax (7,500 words) [view diff] exact match in snippet view article find links to article
conditions – Marfan syndrome, homocystinuria, Ehlers–Danlos syndromes, alpha 1-antitrypsin deficiency (which leads to emphysema), and Birt–Hogg–Dubé syndromeLiver (10,271 words) [view diff] no match in snippet view article find links to article
are also many pediatric liver diseases, including biliary atresia, alpha-1 antitrypsin deficiency, alagille syndrome, progressive familial intrahepaticLung cancer (9,708 words) [view diff] no match in snippet view article find links to article
corticosteroids. Other inflammatory lung and immune system diseases such as alpha-1 antitrypsin deficiency, interstitial fibrosis, scleroderma, Chlamydia pneumoniaeCongenital hypofibrinogenemia (2,217 words) [view diff] no match in snippet view article find links to article
general recommendations for patients with liver disease, particularly Alpha 1 antitrypsin deficiency-associated liver disease. In the latter disease, autophagyFrédéric Chopin (15,312 words) [view diff] exact match in snippet view article find links to article
possibilities advanced have included cystic fibrosis, cirrhosis, and alpha 1-antitrypsin deficiency. A visual examination of Chopin's preserved heart (theDeaths in May 1989 (2,012 words) [view diff] no match in snippet view article find links to article
granddaughter of Charles Darwin. John Cipollina, 45, American guitarist, alpha-1 antitrypsin deficiency. George C. Homans, 78, American sociologist, founder ofDeaths in December 2015 (12,099 words) [view diff] exact match in snippet view article find links to article
52, American model and actor (The Lost Boys, Thrashin', Wired), alpha 1-antitrypsin deficiency. Freda Meissner-Blau, 88, Austrian politician, founderList of Mystery Diagnosis episodes (21 words) [view diff] no match in snippet view article find links to article
breath. Featuring trigeminal neuralgia, polycystic ovary syndrome and alpha-1 antitrypsin deficiency. 6 6 "Blood & Fire" November 11, 2005 (2005-11-11) A 12-year-oldList of skin conditions (17,965 words) [view diff] no match in snippet view article find links to article
syndrome, Lawrence–Seip syndrome) Adiposis dolorosa (Dercum's disease) Alpha-1 antitrypsin deficiency panniculitis (alpha1-protease deficiency panniculitisList of EastEnders characters (2023) (11,428 words) [view diff] no match in snippet view article
her son, Albie Watts (Arthur Gentleman), has the genetic condition Alpha-1 antitrypsin deficiency (AADT). He reassures Sharon that it is not life-threateningLiver support system (15,421 words) [view diff] no match in snippet view article find links to article
important physiological proteins such as albumin, alpha-1-glicoproteine, alpha 1 antitrypsin, alpha-2-macroglobulin, transferrin, globulin tyrosine, and hormonal