المؤلفون: Nahanthiran S; Hospital Tuanku Jaafar Seremban, Department of Pathology, Hematology Unit, Jalan Rasah, Bukit Rasah, 70300, Seremban, Negeri Sembilan, Malaysia. subithira_n@hotmail.com., Nik Mustapha NH; Hospital Tuanku Jaafar Seremban, Department of Pathology, Hematology Unit, Jalan Rasah, Bukit Rasah, 70300, Seremban, Negeri Sembilan, Malaysia., Yasin N; Institute for Medical Research, Cancer Research Centre, Haematology Unit, Setia Alam 40170, Selangor, Malaysia., Idris FB; University Putra Malaysia, Faculty of Medicine and Health Sciences, Department of Pathology, 43400, Serdang, Selangor, Malaysia., Md Noor SB; University Putra Malaysia, Faculty of Medicine and Health Sciences, Department of Pathology, 43400, Serdang, Selangor, Malaysia.

المصدر: The Malaysian journal of pathology [Malays J Pathol] 2024 Aug; Vol. 46 (2), pp. 315-320.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Academy of Medicine of Malyasia, College of Pathologists Country of Publication: Malaysia NLM ID: 8101177 Publication Model: Print Cited Medium: Internet ISSN: 0126-8635 (Print) Linking ISSN: 01268635 NLM ISO Abbreviation: Malays J Pathol Subsets: MEDLINE

مواضيع طبية MeSH: Hemoglobinopathies*/genetics , Hemoglobinopathies*/blood , Hemoglobinopathies*/diagnosis , Hemoglobins, Abnormal*/genetics , Hemoglobins, Abnormal*/analysis, Adolescent ; Female ; Humans ; Male ; Malaysia ; Pedigree

المؤلفون: Pan L; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.; Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Guangxi Medical University, Nanning, China., Qiu Y; Guangxi Key Laboratory of Thalassemia Research, Guangxi Medical University, Nanning, China., Ye L; Department of Clinical Laboratory, Laibin Maternal and Child Health Care Hospital, Laibin, China., Li L; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.; Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Guangxi Medical University, Nanning, China., Huang Y; Department of Clinical Laboratory, Liuzhou Maternal and Child Health Hospital, Liuzhou, China., Mo W; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.; Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Guangxi Medical University, Nanning, China., Lin F; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.; Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Guangxi Medical University, Nanning, China.

المصدر: Laboratory medicine [Lab Med] 2024 Sep 04; Vol. 55 (5), pp. 615-619.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 0250641 Publication Model: Print Cited Medium: Internet ISSN: 1943-7730 (Electronic) Linking ISSN: 00075027 NLM ISO Abbreviation: Lab Med Subsets: MEDLINE

مواضيع طبية MeSH: Hemoglobins, Abnormal*/genetics , Heterozygote*, Humans ; China ; alpha-Thalassemia/genetics ; alpha-Thalassemia/diagnosis ; alpha-Thalassemia/blood ; Male ; Female ; Adult ; Chromatography, High Pressure Liquid ; Electrophoresis, Capillary ; Erythrocyte Indices

المؤلفون: Ge Y; Department of Clinical Laboratory, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China., Zheng G; Department of Clinical Laboratory, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China.; KingMed School of Laboratory Medicine, Guangzhou Medical University, Guangzhou, Guangdong, China., Xian L; Department of Clinical Laboratory, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China., Luo Y; Department of Clinical Laboratory, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China., Liu J; Department of Clinical Laboratory, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China., Lin T; Department of Clinical Laboratory, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China., Cui W; Department of Clinical Laboratory, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China., Yang Y; Department of Clinical Laboratory, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China., Shan H; Department of Clinical Laboratory, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China.

المصدر: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Sep; Vol. 12 (9), pp. e70012.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print Cited Medium: Internet ISSN: 2324-9269 (Electronic) Linking ISSN: 23249269 NLM ISO Abbreviation: Mol Genet Genomic Med Subsets: MEDLINE

مواضيع طبية MeSH: Hemoglobins, Abnormal*/genetics , Phenotype* , Hemoglobinopathies*/genetics , Hemoglobinopathies*/blood , Hemoglobinopathies*/epidemiology , Hemoglobinopathies*/diagnosis, Humans ; Male ; Female ; Adult ; Mutation ; Child ; Erythrocyte Indices ; China ; Adolescent ; Middle Aged

المؤلفون: Amid A; Division of Pediatric Hematology/Oncology, Department of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, BC, Canada., Liu S; Laboratory of Gene Regulation, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.; Chinese Academy of Medical Sciences Oxford Institute, University of Oxford, Oxford, United Kingdom., Babbs C; Laboratory of Gene Regulation, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom., Higgs DR; Laboratory of Gene Regulation, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.; Chinese Academy of Medical Sciences Oxford Institute, University of Oxford, Oxford, United Kingdom.

المصدر: Blood [Blood] 2024 Aug 22; Vol. 144 (8), pp. 822-833.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 7603509 Publication Model: Print Cited Medium: Internet ISSN: 1528-0020 (Electronic) Linking ISSN: 00064971 NLM ISO Abbreviation: Blood Subsets: MEDLINE

مواضيع طبية MeSH: Hydrops Fetalis*/genetics , Hydrops Fetalis*/therapy , Hydrops Fetalis*/etiology , Hydrops Fetalis*/diagnosis , Hemoglobins, Abnormal*/genetics , alpha-Thalassemia*/genetics , alpha-Thalassemia*/therapy , alpha-Thalassemia*/diagnosis, Humans ; Pregnancy

المؤلفون: Satthakarn S; Faculty of Allied Health Sciences, Burapha University, Chonburi 20131, Thailand., Srisuwan W; Department of Medical Technology, School of Allied Health Sciences, University of Phayao, Phayao 56000, Thailand., Kunyanone N; Department of Medical Technology, Chiang Rai Prachanukroh Hospital, Chiang Rai 57000, Thailand., Panyasai S; Department of Medical Technology, School of Allied Health Sciences, University of Phayao, Phayao 56000, Thailand.

المصدر: International journal of molecular sciences [Int J Mol Sci] 2024 Aug 06; Vol. 25 (16). Date of Electronic Publication: 2024 Aug 06.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE

مواضيع طبية MeSH: beta-Globins*/genetics , beta-Thalassemia*/genetics , beta-Thalassemia*/diagnosis , Hemoglobins, Abnormal*/genetics, Adult ; Female ; Humans ; Male ; alpha-Globins/genetics ; Haplotypes ; Mutation ; Electrophoresis, Capillary ; Chromatography, High Pressure Liquid

المؤلفون: Vijian D; Universiti Sains Malaysia, School of Dental Sciences, Department of Medical Microbiology and Parasitology, Health Campus, 16150 Kubang Kerian, Kelantan, Malaysia., Wan Ab Rahman WS; Universiti Sains Malaysia, School of Dental Sciences, Department of Medical Microbiology and Parasitology, Health Campus, 16150 Kubang Kerian, Kelantan, Malaysia. suriana@usm.my., Kannan TP; Universiti Sains Malaysia, School of Dental Sciences, Department of Medical Microbiology and Parasitology, Health Campus, 16150 Kubang Kerian, Kelantan, Malaysia., Zulkafli Z; Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia., Mohd Noor NH; Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia., Bahar R; Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia., Hassan MZ; Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia., Iberahim S; Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia., Abdullah M; Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia., Mohamed Yusoff S; Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia., Ramli M; Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia., Yasin N; Haematology Unit, Cancer Research Centre, Institute for Medical Research, National Institutes of Health, 40170 Shah Alam, Selangor, Malaysia., Esa E; Haematology Unit, Cancer Research Centre, Institute for Medical Research, National Institutes of Health, 40170 Shah Alam, Selangor, Malaysia.

المصدر: The Malaysian journal of pathology [Malays J Pathol] 2024 Aug; Vol. 46 (2), pp. 321-324.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Academy of Medicine of Malyasia, College of Pathologists Country of Publication: Malaysia NLM ID: 8101177 Publication Model: Print Cited Medium: Internet ISSN: 0126-8635 (Print) Linking ISSN: 01268635 NLM ISO Abbreviation: Malays J Pathol Subsets: MEDLINE

مواضيع طبية MeSH: Hemoglobins, Abnormal*/genetics , alpha-Globins*/genetics , alpha-Thalassemia*/genetics , alpha-Thalassemia*/diagnosis , Gene Deletion*, Humans ; Male ; Infant ; Heterozygote ; Malaysia ; Southeast Asian People

المؤلفون: Lugthart G; Leiden University Medical Center (LUMC) Willem-Alexander Children's Hospital, Pediatric Hematology and HSCT, Leiden, The Netherlands., Verweij EJT; Department of Obstetrics and Fetal Therapy, LUMC, Leiden, The Netherlands., Harteveld CL; Department of Clinical Genetics, LUMC, Leiden, The Netherlands., Tan RNGB; LUMC Willem-Alexander Children's Hospital, Neonatal Intensive Care Unit, Leiden, The Netherlands., Knapen MFCM; Department of Obstetrics and Prenatal Medicine, ErasmusMC, Rotterdam, The Netherlands., Slaghekke F; Department of Obstetrics and Fetal Therapy, LUMC, Leiden, The Netherlands., Haak MC; Department of Obstetrics and Fetal Therapy, LUMC, Leiden, The Netherlands., Mohseny AB; Leiden University Medical Center (LUMC) Willem-Alexander Children's Hospital, Pediatric Hematology and HSCT, Leiden, The Netherlands., Smiers FJ; Leiden University Medical Center (LUMC) Willem-Alexander Children's Hospital, Pediatric Hematology and HSCT, Leiden, The Netherlands.

المصدر: American journal of hematology [Am J Hematol] 2024 Aug; Vol. 99 (8), pp. 1613-1615. Date of Electronic Publication: 2024 Apr 24.

نوع المنشور: Letter; Case Reports

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-8652 (Electronic) Linking ISSN: 03618609 NLM ISO Abbreviation: Am J Hematol Subsets: MEDLINE

مواضيع طبية MeSH: alpha-Thalassemia*/genetics , alpha-Thalassemia*/therapy , Hemoglobins, Abnormal*/genetics , Homozygote*, Humans ; Female ; Pregnancy ; Fetal Development ; Oxygen/metabolism ; Adult ; Exchange Transfusion, Whole Blood ; Infant, Newborn

المؤلفون: Gan G, Li W, Huang J, Zheng L, Li T, Li Y

المصدر: Clinical laboratory [Clin Lab] 2024 Jul 01; Vol. 70 (7).

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Clinical Laboratory Publications Country of Publication: Germany NLM ID: 9705611 Publication Model: Print Cited Medium: Internet ISSN: 1433-6510 (Print) Linking ISSN: 14336510 NLM ISO Abbreviation: Clin Lab Subsets: MEDLINE

مواضيع طبية MeSH: Hemoglobins, Abnormal*/genetics , alpha-Globins*/genetics , Electrophoresis, Capillary* , Glycated Hemoglobin*/analysis , Glycated Hemoglobin*/metabolism, Humans ; Chromatography, High Pressure Liquid ; Male ; Female ; Mutation ; DNA Mutational Analysis ; Adult

المؤلفون: Petrovic B; Clinic for Gynecology and Obstetrics, University Clinical Center of Serbia., Milicevic S; Clinic for Gynecology and Obstetrics, University Clinical Center of Serbia.; Faculty of Medicine, University of Belgrade., Sljivancanin D; Clinic for Gynecology and Obstetrics, University Clinical Center of Serbia.; Faculty of Medicine, University of Belgrade., Zdelar Stojanovic L; Clinic for Gynecology and Obstetrics, University Clinical Center of Serbia., Stamenkovic J; Clinic for Gynecology and Obstetrics, University Clinical Center of Serbia.; Faculty of Medicine, University of Belgrade., Grk M; Institute of Human Genetics, Faculty of Medicine, University of Belgrade, Belgrade, Serbia., Dusanovic Pjevic M; Institute of Human Genetics, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

المصدر: Clinical dysmorphology [Clin Dysmorphol] 2024 Jul 01; Vol. 33 (3), pp. 137-144. Date of Electronic Publication: 2024 Feb 16.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE

مواضيع طبية MeSH: Ultrasonography, Prenatal*/methods , Karyotyping*/methods , Abnormal Karyotype* , Fetus*/abnormalities , Fetus*/diagnostic imaging, Humans ; Female ; Pregnancy ; Cross-Sectional Studies ; Adult ; Chromosome Aberrations

المؤلفون: Okubo S; Department of Neurology, Tokyo Teishin Hospital, Japan., Tamagawa T; Department of Neurology, Tokyo Teishin Hospital, Japan., Yamada M; Department of Neurology, Tokyo Teishin Hospital, Japan., Bannai T; Department of Neurology, Tokyo Teishin Hospital, Japan., Seki T; Department of Neurology, Tokyo Teishin Hospital, Japan., Usuki K; Department of Hematology, NTT Medical Center Tokyo, Japan., Shiio Y; Department of Neurology, Tokyo Teishin Hospital, Japan.

المصدر: Internal medicine (Tokyo, Japan) [Intern Med] 2024 Jul 01; Vol. 63 (13), pp. 1929-1932. Date of Electronic Publication: 2023 Nov 20.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Japanese Society of Internal Medicine Country of Publication: Japan NLM ID: 9204241 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1349-7235 (Electronic) Linking ISSN: 09182918 NLM ISO Abbreviation: Intern Med Subsets: MEDLINE

مواضيع طبية MeSH: Cerebral Infarction*/diagnostic imaging , Cerebral Infarction*/diagnosis , Cerebral Infarction*/etiology , Cerebral Infarction*/complications , Hemoglobins, Abnormal*/genetics, Humans ; Male ; Acute Disease ; Middle Aged ; Asymptomatic Diseases