M. Suchi

发表

Diagnosis and localization of focal congenital hyperinsulinism by 18F-fluorodopa PET scan.

Janet R. Saffer, A. Alavi, C. Stanley, 2007, The Journal of pediatrics.

Histopathology of Congenital Hyperinsulinism: Retrospective Study with Genotype Correlations

C. Stanley, A. Ganguly, C. Macmullen, 2003, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Extremes of Clinical and Enzymatic Phenotypes in Children With Hyperinsulinism Caused by Glucokinase Activating Mutations

C. Stanley, C. Buettger, F. Matschinsky, 2009, Diabetes.

An autoinflammatory disease due to homozygous deletion of the IL1RN locus.

U. Broeckel, M. Hessner, J. Verbsky, 2009, The New England journal of medicine.

Diffuse Midline Glioma With Osseous Metastases at Diagnosis: A Case Report

D. Ellison, N. Bhatt, Andrew B. Foy, 2019, Journal of pediatric hematology/oncology.

Ganglioglioma in a Survivor of Infantile Glioblastoma

M. Snuderl, M. Lawlor, J. Serrano, 2020, Journal of pediatric hematology/oncology.

Molecular cloning of human UMP synthase.

N. Harada, K. Okajima, Y. Wada, 1988, Advances in experimental medicine and biology.

Isolation of cDNA clones encoding human acid sphingomyelinase: occurrence of alternatively processed transcripts.

R. Desnick, O. Levran, K. Sandhoff, 1989, The EMBO journal.

Human acid sphingomyelinase. Isolation, nucleotide sequence and expression of the full-length and alternatively spliced cDNAs.

R. Desnick, E. Schuchman, K. Sandhoff, 1991, The Journal of biological chemistry.

Molecular cloning and structural characterization of the human histidase gene (HAL).

Y. Wada, M. Suchi, H. Sano, 1995, Genomics.

Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation.

C. Stanley, A. Ganguly, C. Macmullen, 2004, The Journal of clinical endocrinology and metabolism.

ALK+ histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition.

Michael M. Henry, F. Feuerhake, K. Ernestus, 2021, Blood.

Noncardiogenic pulmonary edema as the chief manifestation of a pheochromocytoma: a case report of MEN 2A with pedigree analysis of the RET proto-oncogene.

M. E. Hodgson, M. Suchi, Y. Okada, 1999, The Tohoku journal of experimental medicine.

Fetal Lung Interstitial Tumor (FLIT): A Proposed Newly Recognized Lung Tumor of Infancy to Be Differentiated From Cystic Pleuropulmonary Blastoma and Other Developmental Pulmonary Lesions

Gretchen M. Williams, M. Dishop, J. Priest, 2010, The American journal of surgical pathology.

Isolation of a rat histidase cDNA sequence and expression in Escherichia coli--evidence of extrahepatic/epidermal distribution.

M. E. Hodgson, K. Asai, Y. Wada, 1997, European journal of biochemistry.

A Rare Case Of a 2-year-old Boy With Alagille Syndrome and Type 3 Hereditary Hemochromatosis With TFR2 Mutation.

Ammar Abdulaziz Khayat, B. Vitola, M. Suchi, 2019, Journal of pediatric gastroenterology and nutrition.

Molecular cloning of a cDNA encoding human histidase.

N. Harada, Y. Wada, Y. Takagi, 1993, Biochimica et biophysica acta.

Molecular characterization of histidinemia: identification of four missense mutations in the histidase gene

K. Asai, S. Sumi, A. Moriyama, 2005, Human Genetics.

Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism

C. Stanley, A. Ganguly, C. Macmullen, 2006, Modern Pathology.

Evaluation and Treatment of Musculoskeletal Vascular Anomalies in Children : An Update and Summary for Orthopaedic Surgeons

J. Meyer, J. Dormans, D. Johnston, 2001 .

Congenital Hyperinsulinism: Intraoperative Biopsy Interpretation Can Direct the Extent of Pancreatectomy

C. Stanley, A. Ganguly, C. Macmullen, 2004, The American journal of surgical pathology.

Lingual Hamartoma Associated with a Cleft Palate in a Newborn

R. Chun, O. Daramola, M. Suchi, 2014, Ear, nose, & throat journal.

Chromophobe renal cell carcinoma in a pediatric living-related kidney transplant recipient.

J. Biegel, M. Sellers, K. Meyers, 2005, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Pancreatic Histopathology of Hyperinsulinism

E. Ruchelli, T. Bhatti, M. Suchi, 2012 .

Successful Treatment of Invasive Conidiobolus Infection During Therapy for Acute Lymphoblastic Leukemia.

S. Kehl, T. Walsh, A. Huppler, 2017, Journal of pediatric hematology/oncology.

Retroviral-mediated transfer of the human acid sphingomyelinase cDNA: correction of the metabolic defect in cultured Niemann-Pick disease cells.

E. Gilboa, R. Desnick, E. Schuchman, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Toward gene therapy for Niemann-Pick disease (NPD): separation of retrovirally corrected and noncorrected NPD fibroblasts using a novel fluorescent sphingomyelin.

R. Desnick, E. Schuchman, S. Gatt, 1992, Human gene therapy.

Increase of protein synthesis by uridine supplement in lectin-stimulated peripheral blood lymphocytes and EB virus-transformed B cell line of hereditary orotic aciduria type I.

K. Okajima, M. Suchi, M. Yazaki, 1987, The Tohoku journal of experimental medicine.

Characterization of Point Mutations in Two Hereditary Orotic

M. E. Hodgson, K. Okajima, S. Sumi, 2006 .

Multifocal Vulvar Smooth Muscle Tumor with an Unusual Intravascular Growth Pattern and Multiple Local Recurrences in a 10-Year-Old Child: A Diagnostic Dilemma

B. Behmaram, D. Uyar, A. Harrington, 2011, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Bronchogenic cyst in the intradiaphragmatic location.

Tushar Chandra, M. Arca, M. Maheshwari, 2013, WMJ : official publication of the State Medical Society of Wisconsin.

Liver failure and x‐linked immunodeficiency type 47

Donald G Basel, G. Telega, M. Suchi, 2020, Pediatric transplantation.

A model of TH17-associated ileal hyperplasia that requires both IL-17A and IFNγ to generate self-tolerance and prevent colitis

Y. Iwakura, N. Salzman, C. Mayne, 2018, Mucosal Immunology.

Multimodal Therapy Including Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy Can Result in Long-term Disease-free Survival in Pediatric Desmoplastic Small Round Cell Tumor With Extraperitoneal Disease

K. Boyd, S. Firat, K. Turaga, 2020, Journal of pediatric hematology/oncology.

Spheno-Orbital Aneurysmal Bone Cyst in a 10-Month-Old Infant.

S. Lew, N. Zwagerman, Elsa V. Arocho-Quinones, 2018, World neurosurgery.

Identification and expression of five mutations in the human acid sphingomyelinase gene causing types A and B Niemann-Pick disease. Molecular evidence for genetic heterogeneity in the neuronopathic and non-neuronopathic forms.

R. Desnick, E. Schuchman, Tsutomu Takahashi, 1992, The Journal of biological chemistry.

Bone Marrow Suppression Associated With Celiac Disease in a 4-Year-Old Boy

A. Elkadri, J. Kolinski, A. Watson, 2021, ACG case reports journal.

Molecular cloning of the human UMP synthase gene and characterization of point mutations in two hereditary orotic aciduria families.

M. E. Hodgson, K. Okajima, S. Sumi, 1997, American journal of human genetics.

Expanding the Phenotype of ALK-positive Histiocytosis: A Report of 2 Cases

P. North, M. Suchi, Huiya Huang, 2018, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Microsatellite instability in in situ and invasive sporadic breast cancers of Japanese women.

H. Iwata, T. Toyama, H. Iwase, 1996, Cancer letters.

Submucosal Supernumerary Smooth Muscle Coat: A Common Histologic Finding in Mowat–Wilson Syndrome With or Without Hirschsprung Disease

R. Kapur, C. Calkins, M. Suchi, 2020, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

A Case of Necrotizing Epiglottitis Due to Nontoxigenic Corynebacterium diphtheriae

R. Chun, J. Lake, R. Willoughby, 2015, Pediatrics.

Herpes Simplex Virus Esophagitis in Immunocompetent Children: A Harbinger of Eosinophilic Esophagitis?

D. Lerner, M. Suchi, J. Fritz, 2017, Journal of pediatric gastroenterology and nutrition.

Microsatellite instability in sporadic human breast cancers

H. Iwata, T. Toyama, H. Yamashita, 1996, International journal of cancer.

Langerhans cell histiocytosis of the digestive tract identified on an upper gastrointestinal examination

K. Boyd, A. Meyers, M. Suchi, 2016, Pediatric Radiology.

Hereditary orotic aciduria heterozygotes accompanied with neurological symptoms.

H. Togari, Y. Wada, S. Sumi, 1998, Tohoku journal of experimental medicine.

A model of TH17-associated ileal hyperplasia that requires both IL-17A and IFNγ to generate self-tolerance and prevent colitis

Y. Iwakura, N. Salzman, C. Mayne, 2018, Mucosal Immunology.