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208 Possible Causes for (=, Bett, das), gehen, IN, ins

  • Osteoporosis

    ., Bette Caan, Dr.P.H., Jane A. Cauley, Dr.P.H., Rowan T. Chlebowski, M.D., Steven R.[dx.doi.org] Niedrige Serumspiegel der alkalischen Phosphatase (AP) sind das Hauptmerkmal der Erkrankung, aber für die Diagnosestellung häufig alleine nicht ausreichend, da einige weitere[doi.org] Plasma homocyst(e)ine and arterial occlusive diseases: a mini-review.[ods.od.nih.gov] Wahl DA, Cooper C, Ebeling PR, Eggerrsdorfer M, Hilger J, Hoffmann K, Josse R, Kanis JA, Mithal A, Pierroz DD, Stenmark J, Stöcklin E, Dawson-Hughes B (2102) A global representation[doi.org] Bernardo , Diretrizes da Sociedade Brasileira de Reumatologia para diagnóstico e tratamento da osteoporose em homens , Revista Brasileira de Reumatologia , 10.1016/j.rbr.2017.06.002[doi.org] Das klinische Spektrum der HPP zeigt eine große Variabilität und reicht von lebensbedrohlichen kindlichen Formen bis hin zu milden Formen mit Manifestation im Erwachsenenalter[doi.org]

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  • Rheumatoid Arthritis

    Niereninsuffizienz First Online: 15 June 2007 Zusammenfassung Entzündliche rheumatische Gelenkerkrankungen außerhalb von systemischen Vaskulitiden und Lupus erythematodes gehen[doi.org] Schmader KE, Oxman MN, Levin MJ, Johnson G, Zhang JH, Betts R, et al.[doi.org] (DAS-28-ESR 3.2-5.1) and high disease activity score (DAS-28-ESR 5.1) were 38% and 7.6%, respectively.[ncbi.nlm.nih.gov] Boshuizen, Ines Rupp, Huibert J. Dinant and Geertrudis A. M.[doi.org] Betts, Kevin Douglas, Ella Xiaoyan Du and Arijit Ganguli , Systematic Literature Review and Meta-analysis of Tumor Necrosis Factor–Alpha Experienced Rheumatoid Arthritis ,[doi.org] 22 Feb 2005 Londonderry, Northern Ireland - The Disease Activity Scale (DAS) 28, a shortened form of the DAS that excludes the ankles and feet, is widely used as an indicator[web.archive.org]

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  • Schizophrenia

    [Patientmodifizierte medikation: Wie gehen schizophrene patienten mit ihren neuroleptika um?][ncbi.nlm.nih.gov] Aylward , E , Walker , E , Bettes , B ( 1984 ). Intelligence in schizophrenia: meta-analysis of the research . Schizophrenia Bulletin 10 , 430 – 459 .[doi.org] The current view on the dopamine (DA) hypothesis of schizophrenia postulates a cortical/subcortical imbalance: subcortical mesolimbic DA projections might be hyperactive,[ncbi.nlm.nih.gov] Third, although the pre- vious meta-analysis included subanalyses that exam- ined IQ by narrower age bands, only three studies were included in the meta-analysis that assessed[web.archive.org] PubMed View Article Google Scholar Betts KS, Williams GM, Najman JM, Scott J, Alati R.[doi.org] […] psychoeducation focused on nutritional counseling, caloric expenditure, and portion control; behavioral self-management including motivational enhancement; goal setting; regular weigh-ins[dx.doi.org]

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  • Acute Myelocytic Leukemia

    Gohring G, Michalova K, Beverloo HB, Betts D, Harbott J, Haas OA, et al.[doi.org] neutropenia.[neupogenhcp.com] Bennett JM , Catovsky D , Daniel MT , Flandrin G , Galton DA , Gralnick HR et al. Proposals for the classification of acute leukaemias.[dx.doi.org] […] the long arm of chromosome 21, that is, del(20)(q11q13)t(20;21)(q11;q11), and in patient 2, material from 21q was inserted into the deleted 20q, that is, del(20)(q11q13)ins[ncbi.nlm.nih.gov] Blood. 2009; 114 :937–951. [ PubMed ] [ Google Scholar ] von Neuhoff C, Reinhardt D, Sander B, Zimmermann M, Bradtke J, Betts D, Zemanova Z, Stary J, Bourquin JP, Haas O,[ncbi.nlm.nih.gov] This aberrant location of AML1/ETO gene and the final karyotype of 45,X,-Y,ins(21;8)(q22;q22q22) could not be determined without molecular analysis.[ncbi.nlm.nih.gov]

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  • Harlequin Ichthyosis

    In früher Kindheit können sie lebensbedrohlich sein und gehen oft mit einer ausgeprägten Entzündung der Haut und einem deutlich erhöhten Wasserverlust einher ( 29 ].[link.springer.com] The impact of the condition on sufferers the Bowen sisters and the Betts sisters can be seen in the Channel 5 documentary 'The Girls With Too Much Skin'.[justgiving.com] […] for an ichthyosis type in humans called autosomal recessive congenital ichthyosis (ARCI). de Wir haben kürzlich ein solches Modell für kongenitale Ichthyosen entwickelt, das[de.glosbe.com] Streicher and Patrick Phillips Published 29m at 6:25 PM New-look Reds rally for 5-3 win over Pirates on Dietrich HR Derek Dietrich's three-run homer in the bottom of the seventh inning[fox19.com] Manuel Tonigold, Annette Rossmann, Marie Meinold, Michael Bette, Melanie Märken, Katharina Henkenius, Anne C. Bretz, Gavin Giel, Chengzhong Cai, Fiona R.[doi.org] Zusammenfassung Ichthyosen sind genetisch verursachte, chronische, das heißt lebenslang bestehende Hautkrankheiten, die durch eine universelle, das gesamte Hautorgan betreffende[link.springer.com]

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  • Mycobacterium Tuberculosis

    Maher , Ziad Khatib , Bette K. Kleinschmidt-DeMasters , David Samuel , Sabine Mueller , Anuradha Banerjee , Jennifer L.[doi.org] Da Wikimedia Commons, l'archivio di file multimediali liberi Jump to navigation Jump to search Wikispecies has an entry on: Mycobacterium tuberculosis .[commons.wikimedia.org] Hao Li, Shuling Liu, Ying Yin, Shuang Ji, Dayong Dong, Jun Zhang, Ling Fu, Junjie Xu and Wei Chen , High-level Expression ofMycobacterium tuberculosisProtein EspB inE. coliand[doi.org] Fenhalls G , Stevens L, Moses L, Bezuidenhout J, Betts JC, van Helden P, et al.[clinchem.aaccjnls.org] Da Wikispecies.[species.wikimedia.org] SEFAYGSFVR 110 120 130 140 TVSLPVGADE DDIKATYDKG ILTVSVAVSE GKPTEKHIQI RSTN 144 16,227 April 16, 2014 - v1 A0C96872035CDDF8 GO Mass spectrometry i Molecular mass is 16100 Da[uniprot.org]

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  • Maturity-Onset Diabetes of the Young

    Drake AJ , Smith A, Betts PR, et al. Type 2 diabetes in obese white children. Arch Dis Child 2002 ; 86 : 207 –8. Owen K , Hattersley AT.[adc.bmj.com] Data were used to build a valid partial least squares discriminate analysis (PLS-DA) model where HNF1A-MODY subjects could be separated from the other diabetes subtypes.[ncbi.nlm.nih.gov] One novel heterozygous mutation (p.Ala2Thr) in INS was identified.[ncbi.nlm.nih.gov] Machado II ; Roberto Teixeira II I Unidade de Endocrinologia do Desenvolvimento, Laboratório de Hormônios e Genética Molecular (LIM-42), Disciplina de Endocrinologia, Hospital das[doi.org] Cavaghan MK, Ehrmann DA, Polonsky KS. Interactions between insulin resistance and insulin secretion in the development of glucose intolerance.[journals.lww.com] We aimed to describe in detail two MODY families with INS mutations. The INS gene was screened by direct sequencing.[ncbi.nlm.nih.gov]

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  • Candidiasis

    Mora-Duarte J, Betts R, Rotstein C, Colombo AL, Thompson-Moya L, Smietana J, Lupinacci R, Sable C, Kartsonis N, Perfect J; Caspofungin Invasive Candidiasis Study Group.[lifeinthefastlane.com] Kaufman DA. Challenging issues in neonatal candidiasis. Curr Med Res Opin . 2010 Jul. 26(7):1769-78. [Medline] . Kaufman DA.[emedicine.medscape.com] Donders, Tinne Caeyers, Priska Tydhof, Ine Riphagen, Thierry van den Bosch and Gert Bellen , Comparison of two types of dipsticks to measure vaginal pH in clinical practice[doi.org] Cornely OA, Lasso M, Betts R, et al. Caspofungin for the treatment of less common forms of invasive candidiasis. J Antimicrob Chemother . 2007 Aug. 60(2):363-9.[web.archive.org] , Revista da Sociedade Brasileira de Medicina Tropical , 50 , 1 , (141) , (2017) .[doi.org] Kaufman DA. Neonatal candidiasis: clinical manifestations, management, and prevention strategies. J Pediatr . Apr 2010. 156 (Suppl 2):S53-S67.[emedicine.medscape.com]

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  • Transient Neonatal Diabetes Mellitus

    Shield JP, Temple IK, Sabin M, Mackay D, Robinson DO, Betts PR, et al.[indianpediatrics.net] Gottschalk ME, Schatz DA, Clare-Salzler M, Kaufman DL, Ting GSP, Geffner ME, Permanent diabetes without serological evidence of autoimmunity after transient neonatal diabetes[link.springer.com] Of the 95% of identifiable mutations for NDM, methylation defects in 6q24, KCNJ11, ABCC8, and INS account for the majority.[ncbi.nlm.nih.gov] Glukosemetabolismus des Neugeborenen von Müttern mit diabetischer Stoffwechsellage, klinische Zeichen der diabetischen Fetopathie und der Hypoglykämie des Neugeborenen, das[karger.com] INS Gene Recessive mutations in the INS gene encoding insulin were discovered to trigger both PNDM and TNDM.[en.wikipedia.org] Fisher DA, Dussault JH, Foley TP, et al. Screening for congenital hypothyroidism: results of screening one million North American infants. J Pediatr 1979; 94:700-705.[siicsalud.com]

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  • Hereditary Multiple Intestinal Atresia

    Sie können in unterschiedlicher Häufigkeit die Speiseröhre, den Magenausgang, Darmabschnitte oder das Anorektum betreffen und gehen häufig mit anderen Fehlbildungen einher[link.springer.com] DELEZIONE 22q11.2 (ESCLUSO: SINDROME DI DIGEORGE, DA CERTIFICARE CON CODICE RCG160 E SINDROME CARDIOFACCIALE DI CAYLER, DA CERTIFICARE CON CODICE RN1770) PALLISTER-KILLIAN[retemalattierare.it] However, a laparotomy still re-ins necessary because it is the only way to confirm thegnosis.[documents.tips] […] resistin and leptin in paediatric chronic renal failure: Correlation with auxological and endocrine profiles Articolo su rivista Vai 2014 Congenital Hyperinsulinism Linked to INS-R[unipa.it] Dies gilt nicht nur für die Therapie, sondern auch für die Nachbetreuung, die für die meisten Atresieformen bis ins Erwachsenenalter erforderlich ist.[link.springer.com] […] nuovo elenco MR esenti Dati tratti dal Supplemento ordinario n. 15 alla GAZZETTA UFFICIALE Serie generale - n. 65 18-3-2017 ALLEGATO 7 (da pag. 247 a pag. 265) CODICE MALATTIA[retemalattierare.it]

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