المؤلفون: Stephanie T. Aronson, Mahmut Y. Celiker, Ludovico Guarini, Rabia Agha

المصدر: Maternal Health, Neonatology and Perinatology, Vol 9, Iss 1, Pp 1-4 (2023)

مصطلحات موضوعية: IVIG, Perinatal infection, Parvovirus B19, Congenital parvovirus infection, Congenital anemia, Fetal anemia, Medicine

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2054-958XTest

الوصول الحر: https://doaj.org/article/0071e5a062d54f70b2ea6cf9d2f57c8aTest

المؤلفون: Ruby Liu, Stephanie M Rice, Seth I. Berger, Christopher Harman, Andrea Quinn, Kelsey Smith, Madhuri Hegde, Huda B. Al-Kouatly, Breanna Valcarcel, Brandy Firman, Elizabeth Critchlow, Mona M. Makhamreh

المصدر: Genetics in Medicine. 23:1325-1333

مصطلحات موضوعية: 0301 basic medicine, Congenital Anemia, Pediatrics, medicine.medical_specialty, business.industry, Genetic counseling, Prenatal diagnosis, Prenatal care, 030105 genetics & heredity, medicine.disease, 03 medical and health sciences, 030104 developmental biology, Hydrops fetalis, medicine, business, Kabuki syndrome, Exome, Genetics (clinical), Exome sequencing

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::db8f9455775f39eb5dd74c1769203498Test
https://doi.org/10.1038/s41436-021-01121-0Test

المؤلفون: Aspesi, Anna, Monteleone, Valentina, Betti, Marta, Actis, Chiara, Morleo, Giulia, Sculco, Marika, Guarrera, Simonetta, Wlodarski, Marcin W., Ramenghi, Ugo, Santoro, Claudio, Ellis, Steven R., Loreni, Fabrizio, Follenzi, Antonia, Dianzani, Irma

المساهمون: Aspesi, Anna*, Monteleone, Valentina, Betti, Marta, Actis, Chiara, Morleo, Giulia, Sculco, Marika, Guarrera, Simonetta, Wlodarski, Marcin W., Ramenghi, Ugo, Santoro, Claudio, Ellis, Steven R., Loreni, Fabrizio, Follenzi, Antonia, Dianzani, Irma

مصطلحات موضوعية: erythroid aplasia, congenital anemia, ribosome

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28931864; info:eu-repo/semantics/altIdentifier/wos/WOS:000411185100063; volume:7; issue:1; firstpage:12010/1; lastpage:12010/8; numberofpages:8; journal:SCIENTIFIC REPORTS; http://hdl.handle.net/2318/1676987Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85029660229; www.nature.com/srep/index.html

الإتاحة: https://doi.org/10.1038/s41598-017-12307-5Test
http://hdl.handle.net/2318/1676987Test

المؤلفون: Maki Yoshihama, Naoya Kenmochi, Tamayo Uechi, 上地 珠代, 剣持 直哉, 吉浜 麻生

المصدر: 日本小児血液・がん学会雑誌 / The Japanese Journal of Pediatric Hematology / Oncology. 2019, 56(5):402

المؤلفون: Steinberg-Shemer, Orna, Keel, Siobán, Dgany, Orly, Walsh, Tom, Noy-Lotan, Sharon, Krasnov, Tanya, Yacobovich, Joanne, Quarello, Paola, Ramenghi, Ugo, King, Mary-Claire, Shimamura, Akiko, Tamary, Hannah

المساهمون: Steinberg-Shemer, Orna*, Keel, Siobán, Dgany, Orly, Walsh, Tom, Noy-Lotan, Sharon, Krasnov, Tanya, Yacobovich, Joanne, Quarello, Paola, Ramenghi, Ugo, King, Mary-Claire, Shimamura, Akiko, Tamary, Hannah

مصطلحات موضوعية: Pediatrics, Perinatology and Child Health, Medicine (all), Hematology, Oncology, congenital anemia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27258031; info:eu-repo/semantics/altIdentifier/wos/WOS:000385523700012; volume:38; issue:7; firstpage:e260; lastpage:e263; numberofpages:4; journal:JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY; http://hdl.handle.net/2318/1677078Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84973304965; http://journals.lww.com/jpho-onlineTest

الإتاحة: https://doi.org/10.1097/MPH.0000000000000587Test
http://hdl.handle.net/2318/1677078Test
http://journals.lww.com/jpho-onlineTest

المؤلفون: Prabhakar Kedar, Rati Devendra, Prashant Warang, Rashmi Dongerdiye, Tejashree Anil More

المصدر: Annals of Hematology. 99:715-727

مصطلحات موضوعية: Male, Models, Molecular, Hemolytic anemia, Congenital Anemia, Iron Overload, Adolescent, Protein Conformation, Hydrops Fetalis, Pyruvate Kinase, Mutation, Missense, India, Biology, Anemia, Hemolytic, Congenital, medicine.disease_cause, Ion Channels, Mice, Structure-Activity Relationship, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, medicine, Animals, Humans, Missense mutation, Computer Simulation, Amino Acid Sequence, Child, Genetic Association Studies, Genes, Dominant, Sanger sequencing, Genetics, Mutation, Anemia, Iron-Deficiency, Sequence Homology, Amino Acid, Genetic disorder, High-Throughput Nucleotide Sequencing, Hematology, General Medicine, medicine.disease, Child, Preschool, 030220 oncology & carcinogenesis, Mutation testing, symbols, Female, Sequence Alignment, Congenital hemolytic anemia, 030215 immunology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::836b608983a796bbc56eee4bae1769c0Test
https://doi.org/10.1007/s00277-020-03955-1Test

المؤلفون: Hideki Muramatsu, Prabhakar Kedar, Rashmi Dongerdiye, Manisha Madkaikar, Etsuro Ito, Seiji Kojima, Hideo Harigae, Yusuke Okuno, Prashant Warang, Tohru Fujiwara

المصدر: International Journal of Hematology. 110:618-626

مصطلحات موضوعية: Congenital Anemia, medicine.medical_specialty, Anemia, Hydrops Fetalis, Genetic counseling, Pyruvate Kinase, India, Pyruvate Metabolism, Inborn Errors, Anemia, Hemolytic, Congenital, Bioinformatics, hemic and lymphatic diseases, Internal medicine, Molecular genetics, Humans, Medicine, Genetic Testing, Glucose Phosphate Isomerase Deficiency, Anemia, Diamond-Blackfan, Genetic testing, Hematology, medicine.diagnostic_test, business.industry, Adenylate Kinase, Glucose-6-Phosphate Isomerase, High-Throughput Nucleotide Sequencing, Anemia, Hemolytic, Congenital Nonspherocytic, medicine.disease, Mutation, Cytokines, business, Pyruvate kinase deficiency

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeaf06ffd2ef8e2eaf70d7a1ed105983Test
https://doi.org/10.1007/s12185-019-02716-9Test

المؤلفون: Hannah Tamary, Orna Steinberg-Shemer

المصدر: Molecular diagnosistherapy. 24(4)

مصطلحات موضوعية: 0301 basic medicine, Congenital Anemia, Genetic counseling, Thalassemia, medicine.medical_treatment, Splenectomy, Prenatal diagnosis, Genetic Counseling, Bioinformatics, 03 medical and health sciences, 0302 clinical medicine, Prenatal Diagnosis, Genetics, Medicine, Humans, Genetic Testing, Pathology, Molecular, Genetic testing, Pharmacology, medicine.diagnostic_test, business.industry, Complete blood count, High-Throughput Nucleotide Sequencing, Anemia, General Medicine, medicine.disease, Hemoglobinopathies, 030104 developmental biology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Molecular Medicine, Bone marrow, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d739cd522302fa2cf0e96c73061958eTest
https://pubmed.ncbi.nlm.nih.gov/32557003Test

المؤلفون: Tanya Krasnov, Orly Dgany, Hannah Tamary, Peretz Resnitzky, Dina Shaft, Joseph Kapelushnik, Hanna Shalev

المصدر: European Journal of Haematology. 99:366-371

مصطلحات موضوعية: Congenital Anemia, Pathology, medicine.medical_specialty, Erythroblasts, Biology, law.invention, Congenital dyserythropoietic anemia type I, 03 medical and health sciences, 0302 clinical medicine, Bone Marrow, law, hemic and lymphatic diseases, medicine, Humans, Founder mutation, Anemia, Dyserythropoietic, Congenital, Microscopy, Invagination, Erythroid Hyperplasia, Hematology, General Medicine, medicine.disease, Microscopy, Electron, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Bone marrow, Electron microscope, Large group, 030215 immunology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa2f24edbfb7c61c621749e18cb53455Test
https://doi.org/10.1111/ejh.12931Test

المؤلفون: Canan Vergin, Yeşim Oymak, Salih Gözmen, Sultan Aydin Köker, Paola Bianchi, Elisa Fermo, Tuba Hilkay Karapınar

المصدر: Journal of Pediatric Hematology/Oncology. 40:e421-e423

مصطلحات موضوعية: Male, 0301 basic medicine, Congenital Anemia, Ineffective erythropoiesis, Hemolytic anemia, Adolescent, Congenital dyserythropoietic anemia type II, Anemia, Vesicular Transport Proteins, Anemia, Hemolytic, Congenital, Hereditary Hemolytic Anemia, medicine.disease_cause, 03 medical and health sciences, 0302 clinical medicine, medicine, Humans, Anemia, Dyserythropoietic, Congenital, business.industry, High-Throughput Nucleotide Sequencing, Hematology, Normocytic anemia, medicine.disease, 030104 developmental biology, Molecular Diagnostic Techniques, Oncology, Chronic Disease, Mutation, Pediatrics, Perinatology and Child Health, Immunology, Congenital dyserythropoietic anemia, business, 030215 immunology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f96bf266fa8bb0660d63fd4a0bbd42dTest
https://doi.org/10.1097/mph.0000000000001207Test