Search

Search Constraints

You searched for: Author/Creator Harroche, Annie

Search Results

1. A retrospective analysis of discordances between international normalized ratio (INR) self‐testing and INR laboratory testing in a pediatric patient population. (8th July 2021)

2. ATP6V0A2‐related cutis laxa in 10 novel patients: Focus on clinical variability and expansion of the phenotype. Issue 10 (20th August 2018)

3. Clinical variability and probable founder effect in oculocutaneous albinism type 7. Issue 3 (6th November 2019)

4. Congenital factor XIII deficiency: comprehensive overview of the FranceCoag cohort. (14th August 2019)

5. Consensus guideline for the diagnosis and management of mannose phosphate isomerase‐congenital disorder of glycosylation. Issue 4 (21st April 2020)

6. Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): study protocol for a multicentric French national observational cross-sectional study. Issue 7 (25th July 2018)

7. Effectiveness of long‐term prophylaxis using pdFVIII/VWF concentrate in patients with inherited von Willebrand disease. (29th April 2022)

9. Gastrointestinal bleeding from angiodysplasia in von Willebrand disease: Improved diagnosis and outcome prediction using videocapsule on top of conventional endoscopy. (29th November 2020)

10. Gynecological and obstetric outcome in the French cohort of women with factor XIII deficiency. Issue 191 (July 2020)