Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 14 (of 14 Records) |
Query Trace: Fetal And Neonatal Alloimmune Thrombocytopenia[original query] |
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Compound heterozygosity of HLA-DRB3*01:01 and HLA-DRB4*01:01 as a potential predictor of fetal neonatal alloimmune thrombocytopenia. Transfusion 2013 Feb 53 (2): 344-52. Loewenthal Ron, Rosenberg Nurit, Kalt Rivka, Dardik Rima, Landau Meytal, Yahalom Vered, Avishai Ofelia, Frenkel Orit, Gazit Ephraim, Steinberg David M, Lipitz Shlomo, Salomon Ophi |
Human platelet antigen alleles in 998 Taiwanese blood donors determined by sequence-specific primer polymerase chain reaction. BioMed research international 2013 2013 973789. Pai Shun-Chung, Burnouf Thierry, Chen Jen-Wei, Lin Liang- |
Genotyping of Human Platelet Antigens by BeadChip Microarray Technology. Methods in molecular biology (Clifton, N.J.) 2015 1310 149-65. Bertrand Gerald, Conti Fabia |
Noninvasive fetal genotyping of human platelet antigen-1a using targeted massively parallel sequencing. Transfusion 2015 Jun 55 (6 Pt 2): 1538-44. Wienzek-Lischka Sandra, Krautwurst Annika, Fröhner Vanessa, Hackstein Holger, Gattenlöhner Stefan, Bräuninger Andreas, Axt-Fliedner Roland, Degenhardt Jan, Deisting Christina, Santoso Sentot, Sachs Ulrich J, Bein Greg |
HLA-DRB3*01:01 is a predictor of immunization against human platelet antigen-1a but not of the severity of fetal and neonatal alloimmune thrombocytopenia. Transfusion 2016 Dec . Wienzek-Lischka Sandra, König Inke R, Papenkort Eva-Maria, Hackstein Holger, Santoso Sentot, Sachs Ulrich J, Bein Greg |
Non-invasive Prenatal Diagnosis of Feto-Maternal Platelet Incompatibility by Cold High Resolution Melting Analysis. Advances in experimental medicine and biology 2016 924 67-70. Ferro Marta, Macher Hada C, Noguerol Pilar, Jimenez-Arriscado Pilar, Molinero Patrocinio, Guerrero Juan M, Rubio Amal |
Maternal HLA genotyping is not useful for predicting severity of fetal and neonatal alloimmune thrombocytopenia. British journal of haematology 2016 Oct . Sainio Susanna, Javela Kaija, Tuimala Jarno, Haimila Kat |
Noninvasive prenatal HPA-1 typing in HPA-1a negative pregnancies selected in the Polish PREVFNAIT screening program. Transfusion 2018 9 58 (11): 2705-2711. Orzi?ska Agnieszka, Guz Katarzyna, Uhrynowska Ma?gorzata, D?bska Marzena, Mikula Michal, Ostrowski Jerzy, Ahlen Maria Therese, Husebekk Anne, Brojer E |
Noninvasive prenatal diagnosis by cell-free DNA screening for fetomaternal HPA-1a platelet incompatibility. Transfusion 2018 9 58 (10): 2272-2279. Ferro Marta, Macher Hada C, Fornés Gema, Martín-Sánchez Jesús, Jimenez-Arriscado Pilar, Molinero Patrocinio, Pérez-Simón José A, Guerrero Juan M, Rubio Amal |
From thrombasthenia to next generation thrombocytopenia: Neonatal alloimmune thrombocytopenia induced by maternal Glanzmann thrombasthenia. Pediatric blood & cancer 2018 9 65 (12): e27376. Barg Assaf Arie, Hauschner Hagit, Luboshitz Jacob, Livnat Tami, Straus Tzipi, Levy-Mendelovich Sarina, Lubetsky Aharon, Rosenberg Nurit, Kenet Gi |
HLA-DRB3*01:01 exhibits a dose-dependent impact on HPA-1a antibody levels in HPA-1a-immunized women. Blood advances 2019 3 3 (7): 945-951. Kjeldsen-Kragh Jens, Titze Thomas L, Lie Benedicte Alexandra, Vaage John T, Kjær Met |
Maternal incompatibilities with fetal human platelet alloantigens -1a, -1b and -15 are the main causes of neonatal alloimmune thrombocytopenia in Russia. Terapevticheskii arkhiv 2018 Aug 90 (7): 65-69. Khaspekova S G, Golovkina L L, Donush E K, Golubeva N V, Shustova O N, Mazurov A |
High-Throughput Screening of Blood Donors for Twelve Human Platelet Antigen Systems Using Next-Generation Sequencing Reveals Detection of Rare Polymorphisms and Two Novel Protein-Changing Variants. Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie 2020 2 47 (1): 33-44. Vorholt Stephanie Maria, Hamker Nele, Sparka Hagen, Enczmann Jürgen, Zeiler Thomas, Reimer Tanja, Fischer Johannes, Balz Ve |
COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage. Prenatal diagnosis 2022 2 42 (5): 601-610. Coste Thibault, Vincent-Delorme Catherine, Stichelbout Morgane, Devisme Louise, Gelot Antoinette, Deryabin Igor, Pelluard Fanny, Aloui Chaker, Leutenegger Anne-Louise, Jouannic Jean-Marie, Héron Delphine, Gould Douglas B, Tournier-Lasserve Elisabe |
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- Page last updated:Apr 29, 2024
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