22 results on '"Yaish, Hassan"'
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2. Fetal presentation of congenital dyserythropoietic anemia type 1 with novel compound heterozygous CDAN1 mutations
3. Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study
4. Unexplained extreme hyperbilirubinemia among neonates in a multihospital healthcare system
5. Ferritin in serum and urine: A pilot study
6. Chapter 6 - Nonimmune Neonatal Hemolytic Anemia: Recent Advances in Diagnosis and Treatment
7. Two novel mutations in TMPRSS6 associated with iron-refractory iron deficiency anemia in a mother and child
8. Long-Term Safety and Efficacy of Mitapivat (AG-348), a Pyruvate Kinase Activator, in Patients with Pyruvate Kinase Deficiency: The DRIVE PK Study
9. Health Related Quality of Life and Fatigue in Patients with Pyruvate Kinase Deficiency
10. Data Coming out of the Human Inhibitor PUP Study (HIPS) Reveal 4 Subgroups of Patients with Distinct Antibody Signatures
11. Pklr Intron Splicing-Associated Mutations and Alternate Diagnoses Are Common in Pyruvate Kinase Deficient Patients with Single or No Pklr Coding Mutations
12. Results Update from the DRIVE PK Study: Effects of AG-348, a Pyruvate Kinase Activator, in Patients with Pyruvate Kinase Deficiency
13. Longitudinal Antibody Signatures Following FVIII Replacement Therapy in Previously Untreated Patients with Severe Hemophilia Α- New Insights from the Hemophilia Inhibitor PUP Study (HIPS)
14. Observational Study on Safety and Efficacy of Factor Replacement Therapy in the Management of Von Willebrand Disease Patients - Results from an Ongoing Study with a VWF/FVIII Concentrate
15. Iron Overload Is Highly Prevalent in All Disease Severity States in Pyruvate Kinase Deficiency (PKD)
16. Using a Next Generation Sequencing Panel to Discover the Obscure Causes of Hereditary Hemolytic Anemias
17. Von Willebrand Factor for Menorrhagia: A Survey and Literature Review
18. Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants
19. The Phenotypic Spectrum of Pyruvate Kinase Deficiency (PKD) from the PKD Natural History Study (NHS): Description of Four Severity Groups By Anemia Status
20. Contributors
21. The Clinical Utility Of Next-Generation Sequencing In The Diagnosis Of Hereditary Hemolytic Anemias
22. Pulmonary Hemorrhage in Association with Autoimmune Chronic Active Hepatitis
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