Ah Reum Diagnosis (2024)

1. [PDF] Richtlijn diagnostiek reumatoïde artritis

  • De NVR/CBO richtlijn 'Diagnostiek en behandeling van Reumatoïde Artritis' stamt uit 2009, gebaseerd op wetenschappelijk evidence tot en met het jaar 2005.

2. Polymyalgia rheumatica en arteriitis temporalis - NHG-Richtlijnen

  • Polymyalgia rheumatica en arteriitis temporalis · Richtlijnen diagnostiek · Richtlijnen beleid · Verwijzing of consultatie · Kernboodschappen · Inleiding ...

  • Naar Volledige tekst ›

3. Lim, Ah Reum - ScholarWorks@Korea University College of Medicine

4. Bloedonderzoek bij reuma | Diagnose

  • Bevat niet: Ah | Resultaten tonen met:Ah

  • Denkt de arts dat je een vorm van reuma hebt? Je arts wil dan soms een bloedonderzoek doen. Een bloedtest laat zien of je misschien reuma hebt.

Bloedonderzoek bij reuma | Diagnose

5. Artritis - NHG-Richtlijnen

  • Artritis · Richtlijnen diagnostiek · Richtlijnen beleid · Belangrijkste wijzigingen · Kernboodschappen · Inleiding · Achtergronden · Richtlijnen diagnostiek.

  • Naar Samenvatting ›

6. Diagnostic delays in rheumatic diseases with associated arthritis

  • Objective : The objective of this study was to determine the length of delay in diagnosis of inflammatory rheumatic diseases, and to indicate the main ...

  • Objective : The objective of this study was to determine the length of delay in diagnosis of inflammatory rheumatic diseases, and to indicate the main factors responsible for such delays. Material and methods : A retrospective multi-centre questionnaire survey carried out among 197 patients...

7. Na Ah-Reum - 0 definities - Encyclo

  • Deze woorden beginnen met `Na`. • Na • na datum • Na de diagnose • Na de repetitie • Na De Wedstrijden • Na dertien jaar • Na dobre i na złe • na drie ...

  • Geen definities gevonden

8. ‪Ah Reum Kang‬ - ‪Google 학술 검색‬

  • Ah Reum Kang. Pai Chai University. arkang.net의 이메일 확인됨 ... Prediction of postoperative complications for patients of end stage renal disease.

  • ‪Pai Chai University‬ - ‪‪인용 횟수 964번‬‬ - ‪Information Security‬ - ‪Data Mining‬

‪Ah Reum Kang‬ - ‪Google 학술 검색‬

9. Refinement of molecular diagnostic protocol of auditory neuropathy ...

  • Mun Young Chang, Ah Reum Kim, Nayoung K.D. Kim, Chung Lee, Woong Yang Park ... Auditory neuropathy spectrum disorder (ANSD) is a sensorineural hearing disorder ...

  • Auditory neuropathy spectrum disorder (ANSD) is a sensorineural hearing disorder caused by dysfunction of auditory neural conduction. ANSD has a heterogeneous etiology, including genetic factors; the response to cochlear implantation significantly varies depending on the etiology. The results of timely cochlear implantation for OTOF-related ANSD (DFNB9) have been reported to be good. Therefore, identifying the causative gene of ANSD, especially OTOF, is an important issue to rehabilitate these patients. Six sporadic ANSD subjects without anatomical abnormality of the cochlear nerve, including the 4 subjects thatwere previously reported to be without detectableOTOFmutation,were included.We performed targeted resequencing (TRS) of known deafness genes and multiphasic bioinformatics analyses of the data that ensured detection of capture failure and structural variations. Exclusion of SNPwas also double checked. The TRS data previously obtained from 2 subjects were reanalyzed. Through this study, we detected 2 mutant alleles of OTOF from 5 (83.3%) of 6 ANSD subjects. All of the 5 subjects carried at least 1 mutant allele carrying p.R1939Q. This variantwas categorized as a simple SNP (rs201326023) in the database and it resided in the exonwith frequent capture failures,which previously led to exclusion of this variant from eligible candidacy mistakenly. In addition,we detected a structural variationwithin OTOF froma previously undiagnosed ANSD subject, which was the second structu...

Refinement of molecular diagnostic protocol of auditory neuropathy ...

10. Your search: "author:Jeong, Ah-Reum" - eScholarship

  • She was treated with resections and has no evidence of disease 3 years after diagnosis. Conclusions. We report a family with a CDKN2A c.301 G>T mutation who ...

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