Molecular diagnostic update in hereditary hemolytic anemia and neonatal hyperbilirubinemia
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Title
Molecular diagnostic update in hereditary hemolytic anemia and neonatal hyperbilirubinemia
Authors
Keywords
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Journal
International Journal of Laboratory Hematology
Volume 41, Issue S1, Pages 95-101
Publisher
Wiley
Online
2019-05-09
DOI
10.1111/ijlh.13014
References
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Related references
Note: Only part of the references are listed.- Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias
- (2018) Roberta Russo et al. AMERICAN JOURNAL OF HEMATOLOGY
- Acute neonatal bilirubin encephalopathy in the State of Utah 2009–2018
- (2018) Robert D. Christensen et al. BLOOD CELLS MOLECULES AND DISEASES
- Hemolysis and Glucose-6-Phosphate Dehydrogenase Deficiency-Related Neonatal Hyperbilirubinemia
- (2018) Michael Kaplan et al. Neonatology
- Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients
- (2018) Andolfo Immacolata et al. AMERICAN JOURNAL OF HEMATOLOGY
- Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan
- (2018) Pei-Chin Lin et al. CLINICA CHIMICA ACTA
- Developmental influence of unconjugated hyperbilirubinemia and neurobehavioral disorders
- (2018) Sanjiv B. Amin et al. PEDIATRIC RESEARCH
- Red blood cell PK deficiency: An update of PK-LR gene mutation database
- (2016) Giulia Canu et al. BLOOD CELLS MOLECULES AND DISEASES
- Clinical utility of next-generation sequencing in the diagnosis of hereditary haemolytic anaemias
- (2016) Archana M. Agarwal et al. BRITISH JOURNAL OF HAEMATOLOGY
- Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases
- (2016) Manu Jamwal et al. CLINICA CHIMICA ACTA
- New insights on hereditary erythrocyte membrane defects
- (2016) Immacolata Andolfo et al. HAEMATOLOGICA
- Glucose-6-Phosphate Dehydrogenase Deficiency
- (2016) Lucio Luzzatto et al. HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA
- New insights on hereditary erythrocyte membrane defects
- (2016) Immacolata Andolfo et al. HAEMATOLOGICA
- Erythrocyte pyruvate kinase deficiency: 2015 status report
- (2015) Rachael F. Grace et al. AMERICAN JOURNAL OF HEMATOLOGY
- Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis
- (2015) E. Glogowska et al. BLOOD
- Disorders of erythrocyte volume homeostasis
- (2015) E. Glogowska et al. International Journal of Laboratory Hematology
- Rare hereditary red blood cell enzymopathies associated with hemolytic anemia - pathophysiology, clinical aspects, and laboratory diagnosis
- (2014) P. Koralkova et al. International Journal of Laboratory Hematology
- Causes of hemolysis in neonates with extreme hyperbilirubinemia
- (2014) R D Christensen et al. Journal of Perinatology
- Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
- (2013) I. Andolfo et al. BLOOD
- Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders
- (2013) Lydie Da Costa et al. BLOOD REVIEWS
- A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: a rare case of autosomal-recessive hereditary spherocytosis due to alpha-spectrin deficiency
- (2013) H M Yaish et al. Journal of Perinatology
- Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels
- (2013) Juliette Albuisson et al. Nature Communications
- Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the “old” and update of the new mutations
- (2012) Angelo Minucci et al. BLOOD CELLS MOLECULES AND DISEASES
- Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver
- (2012) Evita van de Steeg et al. JOURNAL OF CLINICAL INVESTIGATION
- Assessment of UGT Polymorphisms and Neonatal Jaundice
- (2011) Mark G. Bartlett et al. SEMINARS IN PERINATOLOGY
- Peroxiredoxin 2 and Peroxide Metabolism in the Erythrocyte
- (2008) Felicia M. Low et al. ANTIOXIDANTS & REDOX SIGNALING
- Hereditary spherocytosis
- (2008) Silverio Perrotta et al. LANCET
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