Cargando…

P1628: FACTOR XI DEFICIENCY IN CHINESE FEMALE PATIENTS: RESULTS FROM A NATIONWIDE MULTICENTER RETROSPECTIVE STUDY

Detalles Bibliográficos
Autor principal:	Wang, Xiyan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2023
Materias:	Posters
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430050/ http://dx.doi.org/10.1097/01.HS9.0000973384.99796.6d

Ejemplares similares

1628. Treatment Heterogeneity in Pseudomonas aeruginosa Pneumonia
por: Caffrey, Aisling, et al.
Publicado: (2020)

Cancionero de 1628
Publicado: (1945)

Descripcion geografica de America (1628) /
por: Trabulse, Elías
Publicado: (1992)

P1628: ALLOIMMUNIZATION DURING ASSISTED REPRODUCTIVE TECNOLOGY: CASE REPORT OF A PREGNANCY WITH IRREGULAR ANTIBODIES PROBABILY RELATED TO EGG DONOR ANTIGEN.
por: Rolli, M., et al.
Publicado: (2022)

Lrrk2 R1628P variant is a risk factor for essential tremor
por: Chao, Yin Xia, et al.
Publicado: (2015)

Association of LRRK2 R1628P variant with Parkinson’s disease in Ethnic Han-Chinese and subgroup population
por: Zhang, Pei, et al.
Publicado: (2016)

Genetic Analysis of LRRK2 R1628P in Parkinson's Disease in Asian Populations
por: Zhang, Yuan, et al.
Publicado: (2017)

1628 Accuracy of Healthcare Facility-Onset Clostridium difficile Classification
por: Trappler, Regan, et al.
Publicado: (2014)

Entscheidungsbefugnis fur die Durchführung einer Schutzimpfung nach 1628 BGB – kein medizinisches Sachverständigengutachten zur Frage der Impffähigkeit erforderlich: BGB 1628, 1697a
Publicado: (2022)

Relationship between LRRK2 R1628P polymorphism and Parkinson's disease in Asian populations
por: Zhao, Hui, et al.
Publicado: (2016)

Connectivity of corticostriatal circuits in nonmanifesting LRRK2 G2385R and R1628P carriers
por: Zhang, Dongling, et al.
Publicado: (2022)

Factor XI replacement for inherited factor XI deficiency in routine clinical practice: results of the HEMOLEVEN prospective 3-year postmarketing study
por: Bauduer, F, et al.
Publicado: (2015)

Physiology and Transcriptional Analysis of ppGpp-Related Regulatory Effects in Streptomyces diastatochromogenes 1628
por: Song, Yang, et al.
Publicado: (2022)

Obstetric and perioperative management of patients with factor XI deficiency: a retrospective observational study
por: Handa, Shivani, et al.
Publicado: (2022)

LRRK2 G2385R and R1628P Mutations Are Associated with an Increased Risk of Parkinson's Disease in the Malaysian Population
por: Gopalai, Aroma Agape, et al.
Publicado: (2014)

1628P Impact of COVID-19 pandemia on the diagnosis of breast cancer in one region of north of Portugal: One year experience
por: Vilaça, M., et al.
Publicado: (2021)

Management of mild congenital deficiency of Factor XI with a Factor XI inhibitor in pregnancy: A clinical case
por: Murray, Nigel P., et al.
Publicado: (2022)

Identification of factor XI deficiency in Holstein cattle in Turkey
por: Meydan, Hasan, et al.
Publicado: (2009)

Factor XI deficiency diagnosed following use of adalimumab
por: Cetin, Guven, et al.
Publicado: (2014)

Peri- and Postpartum Management of Patients With Factor XI Deficiency
por: Gerber, Gloria F., et al.
Publicado: (2019)

P1077: HODGKIN LYMPHOMA IN PATIENTS WITH HIV: NATIONAL RETROSPECTIVE MULTICENTER STUDY
por: Chekalov, A., et al.
Publicado: (2022)

P663: MULTICENTER, PROSPECTIVE AND RETROSPECTIVE OBSERVATIONAL COHORT STUDY OF PONATINIB IN PATIENTS WITH CML IN ITALY: LONG-TERM FOLLOW-UP RESULTS OF THE OITI TRIAL
por: Breccia, Massimo, et al.
Publicado: (2023)

P654: ALLELIC POLYMORPHISMS OF KIRS AND HLAS PREDICT FAVORABLE ACHIEVEMENT OF TREATMENT-FREE REMISSION IN CML: RESULTS FROM THE POKSTIC TRIAL, MULTICENTER RETROSPECTIVE OBSERVATIONAL STUDY
por: Ureshino, Hiroshi, et al.
Publicado: (2023)

Factor XI deficiency: About 20 cases and literature review
por: Dhaha, Yosra, et al.
Publicado: (2022)

Parkinson-Related LRRK2 Mutation R1628P Enables Cdk5 Phosphorylation of LRRK2 and Upregulates Its Kinase Activity
por: Shu, Yang, et al.
Publicado: (2016)

Heterozygous Cylindromatosis Gene Mutation c.1628_1629delCT in a Family with Brook-Spiegler Syndrome
por: Aguilera, Cintia Arjona, et al.
Publicado: (2016)

Cys482Trp Missense Mutation in the Coagulation Factor XI Gene (F11) in a Korean Patient with Factor XI Deficiency
por: Choi, Seung Jun, et al.
Publicado: (2014)

Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype–phenotype relationship
por: Tiscia, Giovanni L, et al.
Publicado: (2017)

P1032: REAL-LIFE VALIDATION OF MIPSS70: A RETROSPECTIVE MULTICENTER AND NGS ANALYSIS FROM THE GEMFIN DATABASE
por: Hernández-Sánchez, A., et al.
Publicado: (2022)

A Case Report on an Extremely Rare Disease: Factor XI Deficiency
por: Mandal, Shobha, et al.
Publicado: (2020)

P1098: OUTCOME OF FOLLICULAR LYMPHOMA PATIENTS IN MAINTENANCE TREATMENT WITH ANTICD20 MONOCLONAL ANTIBODIES IN SARS-COV2 ERA: RESULTS FROM A MULTICENTER, RETROSPECTIVE- PROSPECTIVE ITALIAN STUDY.
por: Castellino, A., et al.
Publicado: (2022)

Einwilligungszuständigkeit Minderjähriger bei Durchführung einer Coronaschutzimpfung: BGB 630a, 630d, 1626, 1628, 1697a
Publicado: (2022)

Geochemical ice-core constraints on the timing and climatic impact of Aniakchak II (1628 BCE) and Thera (Minoan) volcanic eruptions
por: Pearson, Charlotte, et al.
Publicado: (2022)

P914: VENETOCLAX IN RELAPSE/REFRACTORY AL AMYLOIDOSIS- A MULTICENTER INTERNATIONAL RETROSPECTIVE REAL-WORLD STUDY
por: Lebel, Eyal, et al.
Publicado: (2023)

P1724: QUALITY OF LIFE AND UNMET NEEDS AMONG PH-NEGATIVE MYELOPROLIFERATIVE NEOPLASM PATIENTS: RESULTS OF THE NATIONWIDE SURVEY
por: Ionova, T., et al.
Publicado: (2022)

P05.21. Kangarooing in German neonatology departments: results of a nationwide survey
por: Thiel, M, et al.
Publicado: (2012)

P1166: REPEAT BIOPSY IN RELAPSED OR REFRACTORY DIFFUSE LARGE B CELL LYMPHOMA: A NATIONWIDE SURVEY AND RETROSPECTIVE STUDY
por: Berger, T., et al.
Publicado: (2022)

P1485: A MULTICENTER, RETROSPECTIVE STUDY ON REAL-WORLD EXPERIENCE OF PATIENTS WITH SICKLE CELL DISEASE TREATED WITH VOXELOTOR
por: Andemariam, B., et al.
Publicado: (2022)

Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family
por: Hançer, Veysel Sabri, et al.
Publicado: (2018)

Total hip arthroplasty via the direct anterior approach with Kerboull-type acetabular reinforcement device for an elderly female with factor XI deficiency
por: Sano, Kei, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_pu3qq3kjamueakjcr7l9fup3a5