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AIHAutoimmune Hepatitis
AIHArt Institute of Houston (Texas)
AIHArchitecture in Helsinki (band)
AIHAmerican Institute of Homeopathy
AIHAustralian Institute of Horticulture
AIHArtificial Insemination Husband
AIHArtificial Insemination Homologous (breeding)
AIHAmerican Institute of Hypnotherapy
AIHAssociation Internationale des Hydrogéologues (French: International Association of Hydrogeologists)
AIHAdvanced Image Hosting
AIHAmelogenesis Imperfecta, Hypomaturation Type
AIHAssociation des Internes en Hématologie (French: Association of Interns in Hematology)
AIHAsociación Internacional de Hidatidología (Spanish)
AIHAgence Immobilière Hammami (French; Tunisian real estate agency)
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References in periodicals archive ?
Falk is delighted to partner with Calliditas and to support Calliditas in making Budenofalk oral capsules available as a new treatment option for AIH in the US market.'.
The primary aims of this study were to 1) to conduct a record review of the existing, published WITS patient-created anthology entries to identify common themes associated with lived experiences associated with living with pediatric chronic kidney failure, 2) utilize the findings to educate medical providers about the unique challenges patients face in their disease management, and 3) demonstrate how AIH programming and professionals can be integral to fostering patient healing, coping, personal growth, and resiliency.
A maximum score on the Simplified Diagnostic Criteria for Autoimmune Hepatitis (positive ANA, elevated IgG, compatible histology, and absence of viral hepatitis) confirmed the diagnosis of definite AIH. (2) Furthermore, based on the American College of Rheumatology's Systemic Lupus International Collaborating Clinic (SLICC) score, the patient also met criteria for SLE with at least four criteria (ANA, leucopenia, serositis as per pleural effusion, and low complement).
Multiple genes appear to be implicated in AIH, particularly the human leukocyte antigen (HLA) DR3 haplotype.
Patients were diagnosed with AIH when they met 2 or more of the following criteria: (1) an alanine aminotransferase (ALT) level at least 5-fold the UNL, (2) serum IgG at least 2-fold the UNL or a positive test for smooth muscle antibodies (SMA), and (3) a liver biopsy exhibiting moderate or severe periportal or periseptal lymphocytic piecemeal necrosis.
Here, we report a case of AIH associated with ITP, in which TJLB was useful in making the diagnosis and prompts start of treatment with a corticosteroid.
An ideal model to investigate the mechanisms and treatments of AIH is essential for biological studies.
Considering physiologic data obtained with polysomnography, all three RCT (1-4) revealed significant differences in OMT showing decrease in AIH. It is worth to point out that in one of the studies (3), which also considered subjects with primary snoring and mild OSA, the relevant statistic difference was only for the subjects with moderate OSA.
These pathologic and laboratory findings led to a definitive diagnosis of autoimmune hepatitis (AIH) Type 1.
Autoimmune hepatitis (AIH) is caused by the disorder of self-immune system, which takes the liver cells as their target cells and leads to damage of mainly parenchymal cells in the liver.
Autoimmune liver diseases (AILDs) fall into two broad categories, those with hepatic predominance such as autoimmune hepatitis (AIH) and those with predominance of cholestatic features such as primary biliary cirrhosis (PBC) and primary sclerosing cholangitis (PSC).