Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

A recurrent RYR1 mutation associated with early-onset hypotonia and benign disease course

Subjects: Male; Pathology; Triad

  • Source: Acta Neuropathologica CommunicationsActa Neuropathologica Communications, BioMed Central part of Springer Science, 2021, 9 (1), pp.155.

تفاصيل العنوان

×

European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part III: pharmacological treatment

Subjects: Male; medicine.medical_treatment; Medication

  • Source: European Child and Adolescent PsychiatryEuropean Child and Adolescent Psychiatry, Springer Verlag (Germany), 2021, ⟨10.1007/s00787-021-01899-z⟩Roessner, V, Eichele, H, Stern, J S,

تفاصيل العنوان

×

Family burden of hospital-managed pediatric atopic dermatitis: a nationwide registry-based study

Subjects: Pediatrics; medicine.medical_specialty; family

  • Source: Pediatric Allergy and ImmunologyPediatric Allergy and Immunology, Wiley, 2021, ⟨10.1111/pai.13693⟩Pediatric Allergy and Immunology, 2022, 33 (1), ⟨10.1111/pai.13693⟩Vittrup,

تفاصيل العنوان

×

A large-scale outbreak of hand, foot and mouth disease, France, as at 28 September 2021

Subjects: Pediatrics; medicine.medical_specialty; Epidemiology

  • Source: EurosurveillanceEurosurveillance, European Centre for Disease Prevention and Control, 2021, 26 (43), ⟨10.2807/1560-7917.ES.2021.26.43.2100978⟩Eurosurveillance, 2021, 26 (43),

تفاصيل العنوان

×

Fever during pregnancy as a risk factor for neurodevelopmental disorders: results from a systematic review and meta-analysis

Subjects: Pediatrics; medicine.medical_specialty; Offspring

  • Source: Molecular AutismMolecular Autism, 2021, 12 (1), pp.60. ⟨10.1186/s13229-021-00464-4⟩Molecular Autism, BioMed Central, 2021, 12 (1), ⟨10.1186/s13229-021-00464-4⟩Molecular

تفاصيل العنوان

×
  • 1-10 of  1,422 نتائج ل ""Pediatrics""