S. Ingraham

发表

Renin Angiotensin System Blocker Fetopathy: A Midwest Pediatric Nephrology Consortium Report.

D. Selewski, L. Greenbaum, C. Pan, 2015, The Journal of pediatrics.

hREC2, a RAD51-like gene, is disrupted by t(12;14) (q15;q24.1) in a uterine leiomyoma.

S. Kathiresan, A. Buckler, A. Menon, 1999, Cancer genetics and cytogenetics.

Identification and characterization of novel human transcripts embedded within HMGA2 in t(12;14)(q15;q24.1) uterine leiomyoma.

U. Surti, A. Buckler, J. Rutter, 2006, Mutation research.

Eculizumab exposure in children and young adults: indications, practice patterns, and outcomes—a Pediatric Nephrology Research Consortium study

T. Srivastava, R. Woroniecki, T. Hunley, 2021, Pediatric Nephrology.

Mothball Ingestion in the Setting of G6PD Deficiency Causing Severe Hemolytic Anemia, Methemoglobinemia, and Multiple Organ Failure in a Toddler.

S. Ingraham, P. Purohit, D. Glaser, 2022, Hawai'i journal of health & social welfare.

Insulin and the PI3K/AKT Signaling Pathway Regulate Ribonuclease 7 Expression in the Human Urinary Tract

A. Schwaderer, B. Becknell, J. Spencer, 2017 .

Insulin and the phosphatidylinositol 3-kinase signaling pathway regulate Ribonuclease 7 expression in the human urinary tract.

D. Cohen, S. Tridandapani, A. Schwaderer, 2016, Kidney international.

Association between Ag I -CA Alleles and Severity of Autosomal Recessive Proximal Spinal Muscular Atrophy

J. Carpten, J. Mendell, L. Simard, 2007 .

A YAC contig of the region containing the spinal muscular atrophy gene (SMA): identification of an unstable region.

J. Carpten, J. Wasmuth, C. DiDonato, 1994, Genomics.

Linkage mapping of the spinal muscular atrophy gene

J. Carpten, Z. Kote-Jarai, J. Mendell, 1994, Human Genetics.

Current perspectives on congenital obstructive nephropathy

K. McHugh, S. Ingraham, Susan E. Ingraham, 2011, Pediatric Nephrology.

Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy.

J. McPherson, J. Carpten, B. Wirth, 1994, American journal of human genetics.

Novel Insights on Chronic Kidney Disease , Acute Kidney Injury and Polycystic Kidney Disease 4 Congenital obstructive nephropathy

K. McHugh, S. Ingraham, Susan E. Ingraham, 2017 .

Congenital Obstructive Nephropathy: Clinical Perspectives and Animal Models

K. McHugh, S. Ingraham, Susan E. Ingraham, 2012 .

Struvite urolithiasis and chronic urinary tract infection in a murine model of urinary diversion.

J. Asplin, K. McHugh, B. Bolon, 2013, Urology.

Management and etiology of the unilateral multicystic dysplastic kidney: a review

A. Schwaderer, C. Bates, D. Hains, 2009, Pediatric Nephrology.

Pathogenesis of Renal Injury in the Megabladder Mouse: A Genetic Model of Congenital Obstructive Nephropathy

Daniel A. Hirselj, Monalee Saha, K. McHugh, 2010, Pediatric Research.

Urine Stasis Predisposes to Urinary Tract Infection by an Opportunistic Uropathogen in the Megabladder (Mgb) Mouse

Michael E. Wilhide, B. Becknell, Birong Li, 2015, PloS one.

THE BALANCED, RECIPROCAL TRANSLOCATION OF CHROMOSOMAL SUBBANDS 12q15 AND 14q24 AND ALTERED GENE EXPRESSION IN UTERINE LEIOMYOMA

S. Ingraham, Susan E. Ingraham, 2002 .

Molecular Basis of Renal Adaptation in a Murine Model of Congenital Obstructive Nephropathy

K. McHugh, Michael E. Wilhide, B. Becknell, 2013, PloS one.

Identification of distinct myocardin splice variants in the bladder.

M. Robinson, Monalee Saha, K. McHugh, 2009, The Journal of urology.

A multicopy dinucleotide marker that maps close to the spinal muscular atrophy gene.

J. McPherson, J. Carpten, Z. Kote-Jarai, 1994, Genomics.

Late onset neonatal acute kidney injury: results from the AWAKEN Study

R. Ohls, R. Griffin, P. Brophy, 2018, Pediatric Research.

Association of early dysnatremia with mortality in the neonatal intensive care unit: results from the AWAKEN study

Craig S. Wong, R. Guillet, A. Synnes, 2021, Journal of Perinatology.

Incidence and Risk Factors of Early Onset Neonatal AKI.

C. D’Angio, R. Ohls, R. Griffin, 2019, Clinical journal of the American Society of Nephrology : CJASN.

Incidence and Risk Factors of Early Onset Neonatal AKI.

C. D’Angio, R. Ohls, R. Griffin, 2019, Clinical journal of the American Society of Nephrology : CJASN.

Deletion and conversion in spinal muscular atrophy patients: Is there a relationship to severity?

J. Mendell, R. Moxley, T. Prior, 1997, Annals of neurology.

A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients

T. Crawford, J. Mendell, J. Wasmuth, 1995, Nature Genetics.

Relationship of Patent Ductus Arteriosus Management with Neonatal AKI

Craig S. Wong, R. Guillet, A. Synnes, 2021, Journal of Perinatology.

Documentation of acute kidney injury at discharge from the neonatal intensive care unit and role of nephrology consultation

R. Guillet, A. Synnes, S. Goldstein, 2022, Journal of Perinatology.

The impact of fluid balance on outcomes in premature neonates: a report from the AWAKEN study group

Craig S. Wong, R. Guillet, A. Synnes, 2019, Pediatric Research.

Renal epithelial miR-205 expression correlates with disease severity in a mouse model of congenital obstructive nephropathy

K. McHugh, Michael E. Wilhide, B. Becknell, 2016, Pediatric Research.

The Incidence of Potential Interactions Between Dietary Supplements and Prescription Medications in Cancer Patients at a Veterans Administration Hospital

A. Jazieh, M. Foraida, Alison H Lee, 2006, American journal of clinical oncology.

Beneficial effects of intravenous pamidronate treatment in children with osteogenesis imperfecta under 24 months of age

J. Mahan, S. Ingraham, Rose M Ayoob, 2015, Journal of Bone and Mineral Metabolism.

Calciphylaxis in a pediatric patient with multisystem inflammatory syndrome

S. Ingraham, P. Purohit, Andrew K. Feng, 2023, JAAD case reports.