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3341 - 3350 of 3884 results found

Symptomatischer Ductus arteriosus des Frühgeborenen. S2e-LL (GNPI)

MeSH Terms

Ductus Arteriosus (A07.541.278.395); Ductus Arteriosus (A16.378.303.395)

Guideline Contact
Ina Kopp ([email protected])
English Title Translation
Symptomatic ductus arteriosus in preterm infants
Keywords
Persistierender Ductus arteriosus (PDA), Frühgeborene, Diagnostik des persistierenden Ductus arteriosus, Medikamentöser Ductusverschluss, Chirurgischer Ductusverschluss
Date for Review
15/12/2030
Publication Date
02/04/2026
Expected Publication Date
30/07/2026
Publication Scope
assessment
management
Countries of Application
Germany
Guideline Publication Status
Published
Languages
German
Authors
AWMF (DE)
Publication Year
2026

Symptômes et troubles anxieux chez les jeunes âgés de 12 à 17 ans : repérage, démarche évaluative et diagnostique, traitements, transition de soins et services

MeSH Terms
  • Anxiety Disorders
  • Mental Health
  • Adolescent Psychiatry
  • Disease Management
  • Diagnosis
Guideline Contact
[email protected]
English Title Translation
Symptoms and anxiety disorders in teenagers aged 12 to 17: identification, assessment and diagnostic processes, treatments, transitions in care and services
Publication Date
2026-01-06
Countries of Application
Canada
Guideline Publication Status
Published
Languages
French
Authors
INESSS (CA)
Willingness to Collaborate
Yes
Publication Year
2026

Syndrome de Bardet-Biedl. Guide ALD. Protocole National de diagnostic et de soin pour les maladies rares

MeSH Terms
Congenital; Hereditary; and Neonatal Diseases and Abnormalities (C16); Abnormalities (C16.131); Neurological Disorders / Nervous System Diseases (C10); Central Nervous System Diseases (C10.228)
Publication Scope
management
Countries of Application
France
Guideline Publication Status
Published
Languages
French
Authors
HAS (FR)
Publication Year
2012

Syndrome de Costello. Guide ALD

MeSH Terms
Congenital; Hereditary; and Neonatal Diseases and Abnormalities (C16); Genetic Diseases; Inborn (C16.320); Musculoskeletal Diseases (C05); Musculoskeletal Abnormalities (C05.660)
Publication Scope
assessment
management
Countries of Application
France
Guideline Publication Status
Published
Languages
French
Authors
HAS (FR)
Publication Year
2012

Syndrome de Prader-Willi. Guide ALD

MeSH Terms
Congenital; Hereditary; and Neonatal Diseases and Abnormalities (C16); Genetic Diseases; Inborn (C16.320); Abnormalities (C16.131); Neurological Disorders / Nervous System Diseases (C10); Neurologic Manifestations (C10.597); Nutritional and Metabolic Diseases (C18); Nutrition Disorders (C18.654)
Publication Scope
assessment
management
Countries of Application
France
Guideline Publication Status
Published
Languages
French
Authors
HAS (FR)
Publication Year
2012

Syndrome Gilles de la Tourette

MeSH Terms
Tourette Syndrome (C10.228.140.079.898); Tourette Syndrome (C10.228.662.825.800); Tourette Syndrome (C10.574.500.850); Tourette Syndrome (C16.320.400.820); Tourette Syndrome (F03.550.825.850)
Publication Scope
treatment
Countries of Application
France
Guideline Publication Status
Published
Languages
French
Authors
HAS (FR)
Publication Year
2016

Syndrome néphrotique idiopathique de l'enfant

MeSH Terms
Nephrotic Syndrome (C12.777.419.630.643); Nephrotic Syndrome (C13.351.968.419.630.643); Child (M01.060.406)
Publication Scope
assessment
treatment
Countries of Application
France
Guideline Publication Status
Published
Languages
French
Authors
HAS (FR)
Publication Year
2016

Synkope im Kindes- und Jugendalter. S2k-LL (DGPK)

MeSH Terms

Syncope (C10.597.606.358.800.600); Syncope (C23.888.592.604.359.800.600)

Guideline Contact
Ina Kopp ([email protected])
English Title Translation
Syncope in childhood and adolescence
Date for Review
31/12/2026
Publication Scope
assessment
management
Countries of Application
Germany
Guideline Publication Status
Under Review
Languages
German
Authors
AWMF (DE)
Publication Year
2020