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One Wiki Lab


Júne's One Wiki LAB [OWL] is a collective platform to organize and manage personal & private information of Júne's. This iki is also for providing practical manuals of operating working machines and solving technical problems.

currently accessing from 3.228.220.31 with CCBot/2.0 (https://commoncrawl.org/faq/)



codex de novo prioritas — Updated on 2019/12/24 02:59

  • URL: core.spatio.ml

refero de for de novo — Updated on 2019/12/24 02:59

  • URL: denovo.spatio.ml

refero de .tk .ml .ga cf — Updated on 2018/11/20 03:33

  • URL: nom.spatio.ml

sui hosting Servers — Updated on 2018/08/20 02:12

  • URL: on.spatio.ml

public keys for authorized_keys — Updated on 2018/09/02 01:34

  • URL: ssh.epigen.ml

message of the day (motd) — Updated on 2018/09/02 01:46

  • URL: motd.epigen.ml

scripts for machines — Updated on 2018/09/02 09:07

  • URL: script.epigen.ml

configuration for machines — Updated on 2018/09/07 18:10

  • URL: conf.epigen.ml

Nginx confinguration — Updated on 2018/09/11 15:26

  • URL: nginx.epigen.ml

Router settings for iPTiME routers — Updated on 2019/03/31 19:23



LAB TEST ONLINE — The American Association for Clinical Chemistry (AACC) | 한국어판 — 대한진단검사의학회

Bookmarked

  • Anti-Müllerian HormoneAMH AMH Hormone Test Müllerian-inhibiting Hormone MIH Müllerian Inhibiting Factor MIF Müllerian-Inhibiting Substance MIS

MSD Manual Consumer Version — by MSD | 한국어판

MSD Manual Profession Version — by MSD

Bookmarked


ICD

International Classification of Diseases by WHO, What is it? — ICD

CANCER A-Z

Diabetes

Lupus


Genetic Disorder

Genetic Home Reference — U.S. National Library of Medicine

  • Noonan syndromeNoonan syndrome is a condition that affects many areas of the body. It is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms.
  • Williams syndromeWilliams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, distinctive facial features, and heart and blood vessel (cardiovascular) problems.
  • Duchenne and Becker muscular dystrophyMuscular dystrophies are a group of genetic conditions characterized by progressive muscle weakness and wasting (atrophy). The Duchenne and Becker types of muscular dystrophy are two related conditions that primarily affect skeletal muscles, which are used for movement, and heart (cardiac) muscle. These forms of muscular dystrophy occur almost exclusively in males.

Miltefosine — amebic meningoencephalitis

Oseltamivir — antiviral medication used to treat and prevent influenza A and B

List of Sulfonamides

  • Bacterial infections: eg, sulfamethoxazole/trimethoprim, sulfisoxazole
  • Crohn’s disease: eg, sulfasalazine
  • Diabetes: eg, glyburide, tolbutamide
  • Fluid retention: eg, chlorothiazide, furosemide, hydrochlorothiazide
  • Gout: eg, probenecid
  • High blood pressure: eg, chlorothiazide, hydrochlorothiazide
  • Pain and inflammation: eg, celecoxib
  • Rheumatoid arthritis: eg, sulfasalazine
  • Ulcerative colitis: eg, sulfasalazine.

Amiodarone Oral — antiarrhythmia

Amitriptyline

Ipratropium Bromide Solution


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  • Last modified: 2020/08/04 20:50
  • by Júne Park