Latest Research in Salivary Gland Disorders and Functions

38 research papers · 2026 median publication year

Top Research Topics in Salivary Gland Disorders and Functions

Highest-Cited Papers

  1. Therapeutic potential of haptoglobin in a murine model of sickle cell anemia
  2. THE ROLE OF PERINATAL RISK FACTORS IN THE DEVELOPMENT OF HEMOLYTIC DISEASE IN NEWBORNS
  3. Association of mRNA SARS-CoV-2 vaccination with fatigue and functional recovery in patients with post-acute sequelae of COVID-19 (PASC)
  4. Fabry Disease Screening in Kidney Transplant Recipients: A Single-Center Retrospective Study
  5. Verification of Patient Result Comparability Among Nine Hematology Analyzers Using the CLSI EP31 ‐A‐ IR Guideline: A Four‐Year Experience
  6. Hypokalemia leading to the diagnosis of primary Sjögren’s syndrome: the role of early renal biopsy
  7. Parvovirus B19 infections in paediatric sickle cell disease patients: Genotype and hydroxyurea treatment influence disease severity
  8. Tree-Based Classification of COVID-19 Using NanoString Whole-Blood Immune-Response Profiles: Comparison of Full-Dataset and LOOCV-Embedded Feature Selection
  9. Hydroxyurea dosing in sickle cell anemia: a systematic review, dose-response meta-analysis, and population-level benefit-risk assessment
  10. Mapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades
  11. Endothelin Receptor Antagonism in Sickle Cell Disease: Is the Time Now?
  12. Uncovering the True Genotype: Unusually Severe Sickle Cell Disease in a Child with an Initial HbSC Diagnosis
  13. Polyuria and hypokalemia in an adolescent: deciphering the dual tubulopathy of primary Sjögren’s syndrome - a case report
  14. Nicholas' Story: The Molecular Basis of SCD Pain Crisis
  15. Immunosuppression in children with primary mitochondrial diseases after kidney transplantation: insight from case series of RMND1-related disease
  16. Hemoglobin E Associated with Hemoglobin Constant Spring: Diagnostic Challenges in Heterozygous and Homozygous States
  17. A Case of Isolated Abnormal Behavior Associated With Vitamin B12 Deficiency
  18. Assessment of Interleukin-15 (IL-15) Concentration in Children with Cystic Kidney Disease
  19. The Impact of Severe Albuminuria on the Proinflammatory Monocyte Subset CD14++CD16+ and Antigen-Specific Immune Responses
  20. Efficacy and safety of thalidomide (1 vs 2 mg/kg/d) in transfusion-dependent thalassemia: A Non-Inferiority Trial
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L3 Region - - 2026 Sep Q3

Salivary Gland Disorders and Functions

38 papers

Top Topics (10)

Hemoglobinopathies and Related Disorders15
Salivary Gland Disorders and Functions2
Hemoglobin structure and function1
Blood groups and transfusion1
Long-Term Effects of COVID-191
Lysosomal Storage Disorders Research1
Clinical Laboratory Practices and Quality Control1
Parvovirus B19 Infection Studies1
COVID-19 Clinical Research Studies1
Genomics and Rare Diseases1

Top Publications (20)

1.Therapeutic potential of haptoglobin in a murine model of sickle cell anemia2.THE ROLE OF PERINATAL RISK FACTORS IN THE DEVELOPMENT OF HEMOLYTIC DISEASE IN NEWBORNS3.Association of mRNA SARS-CoV-2 vaccination with fatigue and functional recovery in patients with post-acute sequelae of COVID-19 (PASC)4.Fabry Disease Screening in Kidney Transplant Recipients: A Single-Center Retrospective Study5.Verification of Patient Result Comparability Among Nine Hematology Analyzers Using the CLSI EP31 ‐A‐ IR Guideline: A Four‐Year Experience6.Hypokalemia leading to the diagnosis of primary Sjögren’s syndrome: the role of early renal biopsy7.Parvovirus B19 infections in paediatric sickle cell disease patients: Genotype and hydroxyurea treatment influence disease severity8.Tree-Based Classification of COVID-19 Using NanoString Whole-Blood Immune-Response Profiles: Comparison of Full-Dataset and LOOCV-Embedded Feature Selection9.Hydroxyurea dosing in sickle cell anemia: a systematic review, dose-response meta-analysis, and population-level benefit-risk assessment10.Mapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades11.Endothelin Receptor Antagonism in Sickle Cell Disease: Is the Time Now?12.Uncovering the True Genotype: Unusually Severe Sickle Cell Disease in a Child with an Initial HbSC Diagnosis13.Polyuria and hypokalemia in an adolescent: deciphering the dual tubulopathy of primary Sjögren’s syndrome - a case report14.Nicholas' Story: The Molecular Basis of SCD Pain Crisis15.Immunosuppression in children with primary mitochondrial diseases after kidney transplantation: insight from case series of RMND1-related disease16.Hemoglobin E Associated with Hemoglobin Constant Spring: Diagnostic Challenges in Heterozygous and Homozygous States17.A Case of Isolated Abnormal Behavior Associated With Vitamin B12 Deficiency18.Assessment of Interleukin-15 (IL-15) Concentration in Children with Cystic Kidney Disease19.The Impact of Severe Albuminuria on the Proinflammatory Monocyte Subset CD14++CD16+ and Antigen-Specific Immune Responses20.Efficacy and safety of thalidomide (1 vs 2 mg/kg/d) in transfusion-dependent thalassemia: A Non-Inferiority Trial
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