J. de Chadarévian

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Altered Cellular Distribution and Subcellular Sorting of &ggr;-Tubulin in Diffuse Astrocytic Gliomas and Human Glioblastoma Cell Lines

T. Maraziotis, S. Mörk, L. Del Valle, 2006, Journal of neuropathology and experimental neurology.

Reduction of protein excretion by dimethyl sulfoxide in rats with passive Heymann nephritis.

P. Goodyer, J. S. Fong, B. Kaplan, 1984, Kidney international.

Malignant Peripheral Nerve Sheath Tumor Arising from an Adrenal Ganglioneuroma in a 6-Year-old Boy

C. Katsetos, J. de Chadarévian, J. Pascasio, 2004, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Hemolytic-Uremic Syndrome: Current Concepts and Management

J. S. Fong, B. Kaplan, J. de Chadarévian, 1982 .

Chromosome Rearrangement with No Apparent Gene Mutation in Familial Adenomatous Polyposis and Hepatocellular Neoplasia

A. Ganguly, U. Blecker, J. de Chadarévian, 2002, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Massive infantile nephroblastomatosis. A clinical, radiological, and pathological analysis of four cases

H. Rabinovitch, B. Fletcher, J. de Chadarévian, 1977, Cancer.

Characterization of a Wilms tumor in a 9‐year‐old girl with trisomy 18

V. Huff, J. de Chadarévian, H. Punnett, 2003, American journal of medical genetics. Part A.

An Adolescent With a Mediastinal Mass, Diagnosed With Graves Disease and Thymic Hyperplasia

F. De Luca, J. de Chadarévian, E. Faerber, 2010, Pediatrics.

Coexpression and Accumulation of Ubiquitin +1 and ZZ Proteins in Livers of Children with α1-Antitrypsin Deficiency

S. French, F. V. van Leeuwen, N. Riley, 2002, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Histological Study of Osteoid Osteoma's Blood Supply

M. Herman, C. Katsetos, J. de Chadarévian, 2007, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Hepatocellular ubiquitin expression in alpha1-antitrypsin deficiency.

S. French, J. de Chadarévian, S. S. Wu, 2001, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

T. Seemayer, J. de Chadarévian, C. Osborne, 1985, Human pathology.

Rasmussen encephalitis: complementary role of multitechnique neuroimaging.

J. Hunter, Z. Wang, A. Legido, 1998, AJNR. American journal of neuroradiology.

Sudden death in childhood due to right ventricular dysplasia: report of two cases.

P. Braverman, B. Pawel, J. de Chadarévian, 1994, Pediatric pathology.

Hemolytic-uremic syndrome.

B. Kaplan, J. de Chadarévian, W. L. Robson, 1993, Current problems in pediatrics.

Clinicopathologic Features of Histiocytic Lesions following ALL, with a Review of the Literature

U. Surti, J. Manning, N. Graf, 2010, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Consistency of Isochromosome 7q and Trisomy 8 in Hepatosplenic γδ T-cell Lymphoma: Detection by Fluorescence In Situ Hybridization of a Splenic Touch-Preparation from a Pediatric Patient

M. Koehler, M. Borowitz, C. Griffin, 1999, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Desmoplastic cerebral astrocytoma of infancy: Light microscopy, immunocytochemistry, and ultrastructure

J. de Chadarévian, E. Faerber, J. Pattisapu, 1990, Cancer.

DiGeorge syndrome presenting as severe congenital heart disease in the newborn.

J. Finley, J. de Chadarévian, R. L. Williams, 1977, Canadian Medical Association journal.

Mitochondrial activity in Pompe's disease.

M. Selak, E. Kaye, W. Grover, 2000, Pediatric neurology.

Obliterative segmental sclerosis of pancreatic islets. A possible consequence of hypotensive shock in young BB rats.

T. Seemayer, E. Marliss, J. Yale, 1986, The American journal of pathology.

Malignant Lymphoma Presenting with Nonoliguric Renal Failure

R. Anderson, R. Laxer, J. de Chadarévian, 1983, Clinical pediatrics.

Pulmonary hypertension and HIV infection: new observations and review of the syndrome.

T. E. Schultz, B. Pawel, J. de Chadarévian, 1994, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Down syndrome with low hypodiploidy in precursor B-cell acute lymphoblastic leukemia.

J. Morrissette, J. de Chadarévian, H. Punnett, 2006, Cancer genetics and cytogenetics.

Aberrant localization of the neuronal class III beta-tubulin in astrocytomas.

A. Frankfurter, T. Maraziotis, K. Khalili, 2001, Archives of pathology & laboratory medicine.

Treponemal antigens in congenital and acquired syphilitic nephritis: demonstration by immunofluorescence studies.

J. S. Fong, S. O'regan, K. Drummond, 1976, Annals of internal medicine.

Bone marrow transplantation in lymphomatoid granulomatosis: Report of a case

M. Bernstein, J. de Chadarévian, E. Reece, 1986, Cancer.

Epilepsy, Atherosclerosis, Myocardial Infarction, and Carbamazepine

D. Miles, C. Katsetos, A. Legido, 2003, Journal of child neurology.

ETV6-NTRK3 gene fusion in metastasizing congenital fibrosarcoma.

P. Sorensen, B. Pawel, J. de Chadarévian, 2000, Medical and pediatric oncology.

Pseudotetraploid Clone with Structural Chromosomal Rearrangements in a Chondromyxoid Fibroma: A Case Report

R. Ownbey, J. de Chadarévian, S. Sadri, 2013, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Improvement of pancytopenia and thrombocytopenia with decreasing mosaicism for isochromosome Xp

J. Morrissette, J. de Chadarévian, H. Punnett, 2009, Pediatric blood & cancer.

A newly recognized cause of wheezing: AIDS‐related bronchial leiomyomas

F. d'Amore, G. Isaacson, J. de Chadarévian, 1997, Pediatric pulmonology.

Autosomal dominant inheritance of small kidneys.

P. Kaplan, S. Jéquier, B. Kaplan, 1989, American journal of medical genetics.

Pediatric granular cell tumor of the tracheobronchial tree.

C. Finck, J. de Chadarévian, M. Rozans, 2008, Journal of pediatric surgery.

On the neuronal/neuroblastic nature of medulloblastomas: a tribute to Pio del Rio Hortega and Moises Polak

S. Mörk, L. Del Valle, C. Katsetos, 2002, Acta Neuropathologica.

Milk of calcium cholelithiasis in children.

D. Billmire, E. Smergel, J. de Chadarévian, 2001, Journal of pediatric surgery.

Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathy.

Golder N Wilson, P. Kaplan, F. Frerman, 1989, American journal of medical genetics.

The Mortality of Congenital Diaphragmatic Hernia: Is Total Pulmonary Mass Inadequate, No Matter What?

J. de Chadarévian, F. Guttman, L. Nguyen, 1983, Annals of surgery.

H. Plauchu, J. de Chadarévian, A. Bideau, 1989, American journal of medical genetics.

Maturation of cerebellar neuroblastoma into ganglioneuroma with melanosis. A histologic, immunocytochemical, and ultrastructural study

J. Montes, C. Freeman, A. O’Gorman, 1987, Cancer.

Differential expression and cellular distribution of γ‐tubulin and βIII‐tubulin in medulloblastomas and human medulloblastoma cell lines

A. Giordano, V. Caracciolo, L. D'agostino, 2010, Journal of cellular physiology.

Class III &bgr;-Tubulin Is Constitutively Coexpressed With Glial Fibrillary Acidic Protein and Nestin in Midgestational Human Fetal Astrocytes: Implications for Phenotypic Identity

K. Khalili, L. Del Valle, J. Gordon, 2008, Journal of neuropathology and experimental neurology.

Mesenteric pleomorphic liposarcoma in an adolescent.

B. Pawel, J. de Chadarévian, S. Paul, 1997, Archives of pathology & laboratory medicine.

Hyperdiploidy with trisomy 9 and deletion of the CDKN2A locus in T-cell acute lymphoblastic leukemia.

J. Morrissette, K. Healey, J. de Chadarévian, 2009, Cancer genetics and cytogenetics.

Undifferentiated Embryonal Sarcoma of the Liver is Associated with Mesenchymal Hamartoma and Multiple Chromosomal Abnormalities: A Review of Eleven Cases

N. Gupta, K. Gow, B. Shehata, 2011, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Undifferentiated (embryonal) sarcoma arising in conjunction with mesenchymal hamartoma of the liver.

B. Pawel, J. de Chadarévian, E. Faerber, 1994, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Teratoid Wilms tumor arising as a botryoid growth within a supernumerary ectopic ureteropelvic structure.

B. Pawel, E. Smergel, J. de Chadarévian, 1998, Archives of pathology & laboratory medicine.

Acute poststreptococcal glomerulonephritis mimicking Henoch-Schönlein purpura.

P. Goodyer, B. Kaplan, J. de Chadarévian, 1978, The Journal of pediatrics.

Multiple intestinal atresias associated with angiodysplasia in a newborn.

J. de Chadarévian, R. Prasad, D. Duke, 2011, Journal of pediatric surgery.

Study of an Ovarian Sclerosing Stromal Tumor Presenting as Vaginal Bleeding in a 7-Month-Old

J. Morrissette, J. de Chadarévian, M. Schwartz, 2008, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Terminal Ileal Atresia, Total Colonic Aganglionosis, and Thrombophilia

J. de Chadarévian, M. Peddinghaus, E. Faerber, 2009, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Appendiceal Goblet Cell Metaplasia and Benign Obstructive Mucus Retention in Children: Report of Eight Cases and Review of the Literature

J. de Chadarévian, Miguel A. Guzmán, L. Arthur, 2012, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Metastatic infantile Wilms' tumor and hydrocephalus. A case report with review of the literature

D. Kalousek, J. de Chadarévian, R. Bolande, 1977, Cancer.

The pathology of fibrosing colonopathy of cystic fibrosis: a study of 12 cases and review of the literature.

B. Pawel, J. de Chadarévian, J. Chadarévian, 1997, Human pathology.

Amelioration of murine lupus nephritis by dimethylsulfoxide.

P. Goodyer, B. Kaplan, J. de Chadarévian, 1987, Clinical immunology and immunopathology.

Hereditary Langerhans cell histiocytosis: instances of apparent vertical transmission.

B. Pawel, J. de Chadarévian, 1998, Medical and pediatric oncology.

Renal Giant Cytoplasmic Inclusions in Chédiak-Higashi Syndrome: First Ultrastructural Demonstration in a Human Biopsy

J. de Chadarévian, 2011, Ultrastructural pathology.

De novo circumscribed pulmonary lobar cystic lymphatic anomaly in a young boy. A possible sequela of bronchopulmonary dysplasia.

H. Panitch, J. de Chadarévian, E. Faerber, 1989, Chest.

Diagnosis of "Fetal lung interstitial tumor" requires a FISH negative for trisomies 8 and 2.

J. de Chadarévian, D. Katz, C. Stefanovici, 2011, The American journal of surgical pathology.

Angiocentric CD3+ T-Cell Infiltrates in Human Immunodeficiency Virus Type 1-Associated Central Nervous System Disease in Children

E. Kaye, C. Katsetos, A. Legido, 1999, Clinical Diagnostic Laboratory Immunology.

Relapsing Pancreatitis in Association with Crohn's Disease

E. Seidman, R. Deckelbaum, C. Roy, 1983, Journal of pediatric gastroenterology and nutrition.

Giant cell glioblastoma and pleomorphic xanthoastrocytoma.

S. Mörk, C. Katsetos, A. Legido, 2009, Archives of pathology & laboratory medicine.

Acute glomerulonephritis and hemolytic uremic syndrome.

P. Goodyer, B. Kaplan, J. de Chadarévian, 1980, Canadian Medical Association journal.

Variable expression of autosomal recessive polycystic kidney disease and congenital hepatic fibrosis within a family.

P. Kaplan, P. Russo, S. O'regan, 1988, American journal of medical genetics.

Acute Hypoxia‐Induced Alterations of Calbindin‐D28k Immunoreactivity in Cerebellar Purkinje Cells of the Guinea Pig Fetus at Term

M. Delivoria-Papadopoulos, S. Christakos, C. Katsetos, 2001, Journal of neuropathology and experimental neurology.

Bednar tumor pattern in recurring giant cell fibroblastoma.

D. Coppola, D. Billmire, J. de Chadarévian, 1993, American journal of clinical pathology.

Cerebellar Gliomatosis in a Toddler

J. Ara, J. Piatt, C. Katsetos, 2012, Journal of child neurology.

Trilateral retinoblastoma. Report of two cases.

S. Brownstein, J. de Chadarévian, J. Little, 1984, Archives of ophthalmology.

Hyperdiploidy and trisomy 12 in the cystic partially differentiated nephroblastoma.

D. Billmire, J. de Chadarévian, H. Punnett, 1996, Human pathology.

The Galactocele of Male Infants: An Intriguing Entity. Study and Reflection about a Case, with Review of the Literature

J. de Chadarévian, E. Faerber, D. Duke, 2011, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Truncus arteriosus and other lethal internal anomalies in Goltz syndrome.

D. H. Conway, B. Pawel, J. de Chadarévian, 2000, American journal of medical genetics.

Cytogenetic analysis of a choroid plexus papilloma

J. de Chadarévian, P. Kanev, H. Punnett, 1994, Genes, chromosomes & cancer.

Aniridia/glaucoma and Wilms tumor in a sibship with renal tubular acidosis and sensory nerve deafness.

P. Kaplan, M. Vekemans, B. Kaplan, 1987, American journal of medical genetics. Supplement.

Mycoplasma pneumonia associated with acute glomerulonephritis.

S. O'regan, B. Kaplan, J. de Chadarévian, 1978, Nephron.

Hemolytic-uremic syndrome.

B. Kaplan, J. de Chadarévian, 1994, Canadian Medical Association journal.

Effect of aneuploidy and neoplasia on human ribosomal DNA inheritance.

Golder N Wilson, M. Vekemans, J. de Chadarévian, 1987, American journal of medical genetics. Supplement.

Microtubule-Severing ATPase Spastin in Glioblastoma: Increased Expression in Human Glioblastoma Cell Lines and Inverse Roles in Cell Motility and Proliferation

S. Mörk, J. Janáček, G. Morfini, 2011, Journal of neuropathology and experimental neurology.

Unusual Genetic Aberrations Including a Deletion of KLF6 Tumor Suppressor Gene Revealed by Integrated Cytogenetic Approaches in a Pediatric Ewing Sarcoma

J. White, J. de Chadarévian, J. Pascasio, 2015, Journal of pediatric hematology/oncology.

Three Linked Vasculopathic Processes Characterize Kawasaki Disease: A Light and Transmission Electron Microscopic Study

J. Orenstein, E. Perlman, S. Shulman, 2012, PloS one.

The vascular groove sign: a new CT finding associated with osteoid osteomas.

Patrick T. Liu, J. Kujak, C. Roberts, 2011, AJR. American journal of roentgenology.

Hypercellular/Heterotopic Ganglia in Omphalomesenteric Duct Remnants

S. Coventry, J. de Chadarévian, Sandy S. Wu, 2001, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Double zonal aganglionosis in long segment Hirschsprung's disease with a "skip area" in transverse colon.

J. de Chadarévian, S. Akel, M. Slim, 1982, Journal of pediatric surgery.

The hemolytic uremic syndrome of childhood.

B. Kaplan, J. de Chadarévian, 1978, Perspectives in pediatric pathology.

Hemolytic uremic syndrome with hypocomplementemia, serum C3NeF, and glomerular deposits of C3.

P. Barré, K. Drummond, B. Kaplan, 1977, Archives of pathology & laboratory medicine.

Tetrasomy 13q32.2qter due to an apparent inverted duplicated neocentric marker chromosome in an infant with hemangiomas, failure to thrive, laryngomalacia, and tethered cord.

J. de Chadarévian, M. D. Del Vecchio, J. Pascasio, 2013, Birth defects research. Part A, Clinical and molecular teratology.

Class III beta-tubulin and gamma-tubulin are co-expressed and form complexes in human glioblastoma cells.

P. Baas, Eduarda Dráberová, P. Dráber, 2007, Neurochemical research.

Reciprocal translocation in small-cell sarcomas.

M. Vekemans, T. Seemayer, J. de Chadarévian, 1984, The New England journal of medicine.

Glioneuronal Phenotype in a Diencephalic Pilomyxoid Astrocytoma

C. Katsetos, Goutham Reddy, J. de Chadarévian, 2006, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Hepatocellular Ubiquitin Expression in α1-Antitrypsin Deficiency

S. French, J. de Chadarévian, Sandy S. Wu, 2001 .

Histologic, ultrastructural, and immunocytochemical features of the granulomas seen in a child with the syndrome of familial granulomatous arthritis, uveitis, and rash.

G. Murphy, J. de Chadarévian, S. Raphael, 1993, Archives of pathology & laboratory medicine.

Eleven-year-old girl with acute renal failure, arthritis, hyperuricemia, and family history of rheumatic disorders.

J. de Chadarévian, B. Kaiser, M. Mochon, 1992, The Journal of pediatrics.

Fanconi's anemia, medulloblastoma, Wilms' tumor, horseshoe kidney, and gonadal dysgenesis.

M. Vekemans, J. de Chadarévian, M. Bernstein, 1985, Archives of pathology & laboratory medicine.

Stroke in pediatric HIV infection.

C. Katsetos, A. Legido, J. de Chadarévian, 1999, Pediatric neurology.

Gastric duplication with hemoptysis: CT findings.

J. de Chadarévian, E. Faerber, R. Balsara, 1993, AJR. American journal of roentgenology.

Hemolytic-uremic syndrome.

A. Leung, B. Kaplan, J. de Chadarévian, 1976, Current problems in pediatrics.