Results 201 to 210 of about 33,816 (261)

Diagnosing CAH-X syndrome by long-read sequencing and identifying a novel genotype. [PDF]

Orphanet J Rare Dis
Li Z, Xu S, Fu Q, Du L, Lin Q, Lin H, E H, Liu H.   +7 more
europepmc   +1 more source

Bruised

, 2016
openaire   +1 more source

Type 3 Von Willebrand disease: two clinical cases of a rare disorder. [PDF]

Oxf Med Case Reports
Belcadi Abassi K, Larbi Ouassou K, Radi A, Laaraje A, Babour S, Ait Hmadouch S, Hassani A, Khorassani MEL, Abilkassem R.   +8 more
europepmc   +1 more source

Determinants of Patient Satisfaction with Vascular Access in Hemodialysis: Insights from a Multicenter Study in Italy. [PDF]

Clin Pract
Andretta V, Cascella M, Cerrone A, Prendin A, Mastrangelo A, Cerrone V.   +5 more
europepmc   +1 more source

Experiences of participant engagement from an African and Asian ancestry cohort during a clinical research study of lymph node responses to influenza immunisation in the United Kingdom

Metcalf D, Man NS, Coelho S, Palomeras A, Kim SJ, Marsden BD, Szommer T, Chan TY, Siu JH, Coles M, Dendrou CA, Palmer DB, Vanderslott S, Pollock KM.   +13 more
europepmc   +1 more source