Factor VII Deficiency and Second Trimester Abortion: A Case Report. [PDF]
Nguyen KP, Aqui TLB, Milestone H.
europepmc +1 more source
Expression of recombinant human coagulation factors VII (rFVII) and IX (rFIX) in various cell types, glycosylation analysis, and pharmacokinetic comparison [PDF]
Ernst Böhm +9 more
openalex +1 more source
Coagulation factors II, V, VII, IX, X and XI and mortality – a cohort study
Eng Soo Yap +3 more
openalex +1 more source
Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder
ABSTRACT Objectives We describe the clinical manifestations and developmental abilities of individuals with SYT1‐associated neurodevelopmental disorder (Baker‐Gordon syndrome) from infancy to adulthood. We further describe the neuroradiological and electrophysiological characteristics of the condition at different ages, and explore the associations ...
Sam G. Norwitz +3 more
wiley +1 more source
Perioperative management of severe factor VII deficiency: a single-center experience in China. [PDF]
Zhu C +5 more
europepmc +1 more source
Hospital Readmission After Traumatic Brain Injury Hospitalization in Community‐Dwelling Older Adults
ABSTRACT Objective To examine the risk of hospital readmission after an index hospitalization for TBI in older adults. Methods Using data from the Atherosclerosis Risk in Communities (ARIC) study, we used propensity score matching of individuals with an index TBI‐related hospitalization to individuals with (1) non‐TBI hospitalizations (primary analysis)
Rachel Thomas +7 more
wiley +1 more source
Congenital factor VII deficiency: When to suspect?
Ankit Ranjan +3 more
doaj +1 more source
Preoperative diagnosis and laparoscopic management of Amyand's hernia with isolated factor VII deficiency: A case report. [PDF]
Bajafar A, Mohamed R, Elaagib M, Ali M.
europepmc +1 more source
Prothrombin Complex Concentrate vs Factor VII for Refractory Bleeding in Cardiac Surgery. [PDF]
Hyland SJ +6 more
europepmc +1 more source
Effectiveness and Safety of Nusinersen and Risdiplam in Spinal Muscular Atrophy: A Systematic Review
ABSTRACT Objective Spinal Muscular Atrophy (SMA) is a rare genetic disorder marked by progressive muscle weakness and mobility loss. It has a profound physical, emotional and social impact on patients and caregivers, requiring comprehensive medical and supportive care.
Amin Mehrabian +9 more
wiley +1 more source

