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7,385 Possible Causes for Asymptomatic Hyperammonemia (2- to 5-fold Increase), Italian

Did you mean: Asymptomatic Hyperammonemia (2- to 5-fold Increase, Italian

  • Adrenogenital Syndrome

    […] bab.la Dictionary English-Italian A adrenogenital syndrome "adrenogenital syndrome" translation into Italian EN volume_up adrenogenital syndrome {noun} IT sindrome adrenogenitale[en.bab.la] […] incidence is approximately 1 15,000 ). [6] Continued treatment and wellness is enhanced by education and follow up. [19] History [ edit ] Before 20th century [ edit ] An Italian[en.wikipedia.org] It appears to happen more often in people of Ashkenazi Jewish, Hispanic, Slavic and Italian background. Does CAH go by any other names?[newbornscreening.info]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Familial Mediterranean Fever

    Mediterranean fever is an inherited disorder that usually occurs in people of Mediterranean origin — including those of North African, Jewish, Arab, Armenian, Turkish, Greek or Italian[mayoclinic.org] It has been described in several ethnic groups including Sephardic Jews, Armenians, Turks, North Africans, Arabs, Greeks, and Italians.[ncbi.nlm.nih.gov] Mediterranean fever (FMF) is a disease of people with genetic origins in the Mediterranean basin, predominantly Sephardic Jews, North African Arabs, Armenians, Turks, Greeks, and Italians[msdmanuals.com]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Glycogen Storage Disease Type 1

    PATIENTS AND METHODS: Ninety-five patients (median age at the time of the study: 14.5 years) were enrolled from nine Italian referral centres for metabolic diseases.[ncbi.nlm.nih.gov] Sechi A, Deroma L, Paci S, et al ; Quality of Life in Adult Patients with Glycogen Storage Disease Type I: Results of a Multicenter Italian Study. JIMD Rep. 2013 Dec 21.[patient.info]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Fucosidosis

    This mutation was present in one allele and was found also in the mother who was of Italian origin. (2) A C to A mutation (W382X) in exon 6 in an Italian patient.[ncbi.nlm.nih.gov] This G60D mutation creates a unique site for AflIII. 4) A frameshift mutation resulted from a two-base deletion in exon 2 (K151fs) in an Italian patient.[ncbi.nlm.nih.gov] Abstract A significant proportion of patients affected with fucosidosis have Italian ancestors.[ncbi.nlm.nih.gov]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Benign Adult Familial Myoclonic Epilepsy

    Five Italian BAFME families were identified. One family has not been previously reported.[ncbi.nlm.nih.gov] We have already reported two, and recently observed a third, Italian families with linkage to chromosome 2p11.1-q12.2.[moh-it.pure.elsevier.com] Cell lines are stored at the Galliera Genetic Bank (supported by the Italian Telethon Foundation).[link.springer.com]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Childhood Non-Small Cell Lung Cancer

    […] status assessment significantly predict survival of elderly patients with advanced non-small-cell lung cancer receiving chemotherapy: a prognostic analysis of the multicenter Italian[unipa.it] […] exudative pleural effusions and contributes actively to neutrophil recruitment in the inflamed pleural space Articolo su rivista Vai 2004 Prevalence and management of pain in Italian[unipa.it]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Marchiafava Bignami Disease

    Bignami, Amico, Italian physician, 1862-1929. Marchiafava-Bignami disease - see under Marchiafava Marchiafava, Ettore, Italian pathologist, 1847-1935.[medical-dictionary.thefreedictionary.com] History and etymology The disease was originally described in Italian alcoholic patients by Italian pathologists Ettore Marchiafava and Amico Bignami .[radiopaedia.org] Some of the old literature on MBD suggested that this condition was more common in Italians.[emedicine.medscape.com]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Cooley's Anemia

    Thalassemia is a hereditary disease that affected Italians and Greeks but now is spread over the world.[capegazette.com] Cooley’s anemia is disproportionately represented among people of Italian heritage.[marinolodge.org] The disease was usually seen in children of southern European parentage—Greek, Syrian or Italian peoples—though it has been reported from many other races over the world.[jamanetwork.com]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Vitamin D Deficiency

    The Italian Association of Clinical Endocrinologists appointed a task force to review literature about vitamin D deficiency in adults.[ncbi.nlm.nih.gov] Copyright 2017 The Italian Society of Diabetology, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition, and the Department of Clinical[ncbi.nlm.nih.gov] In the following research we have taken into consideration the results of the monitoring of Vitamin D levels in 46 refugees of the Italian Service for protection of refugees[ncbi.nlm.nih.gov]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • CDK4-linked Melanoma

    CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma.[ncbi.nlm.nih.gov] CDKN2A/CDK4 molecular study on 155 Italian subjects with familial and/or primary multiple melanoma.[ncbi.nlm.nih.gov]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)

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