S. Savelli

发表

Mucoepidermoid carcinoma of the parotid gland as a second malignant neoplasm

A. Termuhlen, S. Savelli, K. Klopfenstein, 2005, Pediatric blood & cancer.

Therapy‐related myeloid neoplasms resembling juvenile myelomonocytic leukemia: a case series and review of the literature

A. Rangaswami, C. Dvorak, G. Dahl, 2021, Pediatric blood & cancer.

Fertility Preservation for Pediatric and Adolescent Patients With Cancer: Medical and Ethical Considerations

M. Fallat, S. Klipstein, S. Savelli, 2020, Pediatrics.

Sensitive and Specific Real-Time Polymerase Chain Reaction Assays to Accurately Determine Copy Number Variations (CNVs) of Human Complement C4A, C4B, C4-Long, C4-Short, and RCCX Modules: Elucidation of C4 CNVs in 50 Consanguineous Subjects with Defined HLA Genotypes

H. Nagaraja, B. Rovin, D. Birmingham, 2007 .

Utility of a screening tool for haemostatic defects in a multicentre cohort of adolescents with heavy menstrual bleeding

S. O’Brien, J. Stanek, S. Ahuja, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

Iron deficiency and fatigue among adolescents with bleeding disorders

J. Stanek, A. Zia, S. Savelli, 2021, American journal of hematology.

Pentostatin for treatment of refractory autoimmune lymphoproliferative syndrome

R. Bajwa, T. Gross, S. Savelli, 2011, Pediatric blood & cancer.

Recommendations for screening for thrombophilic tendencies in teenage females prior to contraceptive initiation.

B. Kerlin, S. Savelli, C. Blanchong, 2006, Journal of pediatric and adolescent gynecology.

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans.

Bi Zhou, H. Nagaraja, B. Rovin, 2007, American journal of human genetics.

Sensitive and specific real-time PCR assays to accurately determine gene copy-number variations (CNVs) of human complement C4A, C4B, C4-Long, C4-Short and RCCX modules: Elucidation of C4 GCNVs in 50 consanguineous subjects with defined HLA genotypes

H. Nagaraja, B. Rovin, C. Y. Yu, 2007 .

Measuring pediatric hematology–oncology fellows’ skills in humanism and professionalism: A novel assessment instrument

R. Jubran, L. Kersun, A. Agrawal, 2017, Pediatric blood & cancer.

Sensitive and Specific Real-Time Polymerase Chain Reaction Assays to Accurately Determine Copy Number Variations (CNVs) of Human Complement C4A, C4B, C4-Long, C4-Short, and RCCX Modules: Elucidation of C4 CNVs in 50 Consanguineous Subjects with Defined HLA Genotypes1

H. Nagaraja, B. Rovin, D. Birmingham, 2007, The Journal of Immunology.

Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus

H. Nagaraja, B. Rovin, D. Birmingham, 2009, Cytogenetic and Genome Research.

Outcomes after bloodstream infection in hospitalized pediatric hematology/oncology and stem cell transplant patients

K. Myers, R. Nagarajan, C. Dandoy, 2019, Pediatric blood & cancer.

Opposite Profiles of Complement in Antiphospholipid Syndrome (APS) and Systemic Lupus Erythematosus (SLE) Among Patients With Antiphospholipid Antibodies (aPL)

H. Nagaraja, Yee-Ling Wu, Chack-Yung Yu, 2019, Front. Immunol..

Autoimmune Lymphoproliferative Syndrome (ALPS): A Case with Congenital Onset

S. Qualman, J. Bleesing, S. Kahwash, 2007, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

An Open-Label, Single-Arm, Efficacy Study of Tranexamic Acid in Adolescents with Heavy Menstrual Bleeding.

S. Vesely, S. O’Brien, S. Ahuja, 2019, Journal of pediatric and adolescent gynecology.