A. Pinto

发表

Undifferentiated rhabdomyosarcoma with lymphoid phenotype expression.

G. Tallini, D. Parham, R. Novak, 1997, Medical and pediatric oncology.

Mesenchymal Hamartoma of the Liver with Inversion of Chromosome 19

S. Shetty, A. Pinto, B. Roland, 2011, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Hyperdiploid karyotype in a choroid plexus papilloma.

A. Pinto, B. Roland, 1996, Cancer genetics and cytogenetics.

Expression of markers shared between human natural killer cells and neuroblastoma lines

R. Mcgarry, A. Pinto, C. Trevenen, 2004, Cancer Immunology, Immunotherapy.

Spinal Cord Involvement in Primary Angiitis of the Central Nervous System

A. Pinto, J. Rocha, M. Teixeira, 2003 .

Mitochondrial abnormalities of liver in two children with citrullinaemia

R. Scott, S. Zamora, H. Parsons, 1997, Journal of Inherited Metabolic Disease.

A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch‐German) Mennonite and Hutterite patients in North America

C. Ober, R. Hegele, V. Siu, 2012, American journal of medical genetics. Part A.

Fatal neonatal pneumonia caused by adenovirus type 35. Report of one case and review of the literature.

T. Jadavji, A. Pinto, R. Beck, 1992, Archives of pathology & laboratory medicine.

Pediatric Surgical Pathology of the Nasopharynx and Sella Turcica

M. Bründler, A. Pinto, 2021, Pediatric Head and Neck Textbook.

Immunohistochemical expression of neuron‐specific enolase and leu 7 in Ewing's sarcoma of bone

M. Schell, D. Parham, F. A. Hayes, 1989, Cancer.

Congenital Extrarenal Non-Central Nervous System Malignant Rhabdoid Tumor

M. Coppes, R. Egeler, J. Wolff, 2002, Journal of pediatric hematology/oncology.

Decreased expression of the INK4 family of cyclin‐dependent kinase inhibitors in Wilms tumor

D. Demetrick, M. Coppes, M. Arcellana‐Panlilio, 2000, Genes, chromosomes & cancer.

Pathobiologic Markers of the Ewing Sarcoma Family of Tumors: State of the Art and Prediction of Behaviour

D. Parham, P. Dickman, A. Pinto, 2010, Sarcoma.

Trisomy 21 and isodicentric chromosome 21 in Kostmann syndrome following treatment with G-CSF.

R. Woodman, A. Pinto, B. Roland, 2001, Cancer genetics and cytogenetics.

Leiomyoma of the esophagus associated with bronchial obstruction owing to inflammatory pseudotumor in a child.

V. Kirk, S. McFadden, G. Boag, 2000, Journal of pediatric surgery.

Recurrent respiratory papillomatosis causing chronic stridor and delayed speech in an 18-month-old boy.

V. Kirk, A. Pinto, D. Drummond, 2006, Canadian respiratory journal.

Argininosuccinic aciduria: Long-term treatment with arginine

R. Scott, R. Carter, A. Pinto, 1987, Journal of Inherited Metabolic Disease.

Fatal Cholestatic Hepatitis in an Infant: An Unusual Etiology

R. Scott, M. Oliver, A. Pinto, 1995 .

Acute hemorrhagic leukoencephalitis in male sibs.

P. Bridge, A. Pinto, D. R. Mcleod, 2002, American journal of medical genetics.

Benign Lymphoepithelial Lesion (Mikulicz's Syndrome) of the Submandibular Glands in a Four-Year-Old Boy

A. L. Wong, A. Leung, W. Robson, 1994 .

Immunohistochemical evaluation of dystrophin expression in small round cell tumors of childhood.

D. Parham, A. Pinto, D. Paslawski, 1993, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Giant cell fibroblastoma in childhood immunohistochemical and ultrastructural study.

A. Pinto, W. Hwang, C. G. Seagram, 1992, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Intractable diarrhea in a newborn infant: microvillous inclusion disease.

R. Scott, M. Robertson, A. Pinto, 2001, Canadian journal of gastroenterology = Journal canadien de gastroenterologie.

Ependymal Abnormalities in Lissencephaly/Pachygyria

H. Darwish, P. Barth, M. Ōsawa, 1993, Journal of Neuropathology and Experimental Neurology.

Druggable targets in pediatric neurocutaneous melanocytosis: Molecular and drug sensitivity studies in xenograft and ex vivo tumor cell culture to identify agents for therapy.

O. Kovalchuk, A. Kirton, Y. Nagashima, 2015, Neuro-oncology.

A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch‐German) Mennonite and Hutterite patients in North America

C. Ober, R. Hegele, V. Siu, 2012, American journal of medical genetics. Part A.