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
Academic Journal

Novel UBQLN2 mutations linked to Amyotrophic Lateral Sclerosis and atypical Hereditary Spastic Paraplegia phenotype through defective HSP70-mediated proteolysis

Subjects: Missense/*genetics; Protein Domains/genetics; Mutation

  • Source: ISSN: 0197-4580 ; Neurobiology of Aging ; https://hal.science/hal-03001781 ; Neurobiology of Aging, 2017, 58, pp.239.e11-239.e20. ⟨10.1016/j.neurobiolaging.2017.06.018⟩.

تفاصيل العنوان

×
Academic Journal

Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis

Subjects: Female; Humans; Male

  • Source: Orphanet journal of rare diseases ; https://univ-lyon1.hal.science/hal-02192909 ; Orphanet journal of rare diseases, 2014, 9, pp.191. ⟨10.1186/s13023-014-0191-8⟩ ; http://www.ojrd.com/

تفاصيل العنوان

×
Academic Journal

Facial Expression Recognition and Emotion Understanding in Children after Neonatal Open-Heart Surgery for Transposition of the Great Arteries

Subjects: Child; Preschool; Cognition Disorders

  • Source: ISSN: 0012-1622 ; Developmental Medicine and Child Neurology ; https://hal.parisnanterre.fr/hal-01423139 ; Developmental Medicine and Child Neurology, 2014, 56 (6), pp.564--571.

تفاصيل العنوان

×