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Anti-foot-and-mouth disease serum
Pirquet serum disease
Serum against allergic diseases
Serum disease
Serum intoxication
Serum reaction
Serum sickness

Translation of "Pirquet serum disease " (English → French) :

Pirquet serum disease | serum sickness
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
maladie du sérum
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
serum sickness | serum disease | serum intoxication | serum reaction
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
maladie sérique | maladie du sérum
médecine > sémiologie et pathologie | biologie > immunologie | médecine > allergologie
médecine > sémiologie et pathologie | biologie > immunologie | médecine > allergologie
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
anti-foot-and-mouth disease serum
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
sérum anti-aphteuse
IATE - AGRICULTURE, FORESTRY AND FISHERIES
IATE - AGRICULTURE, FORESTRY AND FISHERIES
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
serum against allergic diseases
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
sérum anti-allergique
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Nephrotic syndrome with often-early onset defined by severe proteinuria with low serum albumin and possible oedema. This disease is rare but severe as it usually progresses to end-stage renal failure. Mutations in the NPHS2 gene (chromosome 1q25-q31
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome néphrotique idiopathique familial cortico-résistant
SNOMEDCT-BE (chromosome 1q25-q31 / 718141008
SNOMEDCT-BE (disorder) / 718141008
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A very rare secondary neonatal autoimmune disease characterised by generalised weakness, severe hypotonia, absent or reduced deep tendon reflexes and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrop
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
dermatomyosite néonatale
SNOMEDCT-BE (disorder) / 774082004
SNOMEDCT-BE (disorder) / 774082004
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare gastrooesophageal disease characterised by diffusely enlarged gastric folds, excessive mucus secretion, normal serum protein and gastric TGF-alpha levels. Patients typically present anaemia, abdominal pain not related to eating or bowel habits
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
gastropathie hypertrophique sans hypoprotéinémie
SNOMEDCT-BE (disorder) / 773397000
SNOMEDCT-BE (disorder) / 773397000
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Others have searched : pirquet serum disease    anti-foot-and-mouth disease serum    serum against allergic diseases    serum disease    serum intoxication    serum reaction    serum sickness    Pirquet serum disease    


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'Pirquet serum disease'

Date index:2022-01-30 -

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