Search Results - "Chatten, Jane"

Lipoblastoma/Lipoblastomatosis: A Clinicopathologic Study of 25 Tumors by Collins, Margaret H., Chatten, Jane

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Prognostic signs in the surgical management of plexiform neurofibroma: The Children’s Hospital of Philadelphia experience, 1974-1994 by Needle, Michael N., Cnaan, Avital, Dattilo, James, Chatten, Jane, Phillips, Peter C., Shochat, Stephen, Sutton, Leslie N., Vaughan, Sheila N., Zackai, Elaine H., Zhao, Huaqing, Molloy, Patricia T.

“…Objectives: To estimate the rate of progression of plexiform neurofibroma after surgery and to identify prognostic factors that predict progression. Study…”
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Monoclonal antibody NB84 in the differential diagnosis of neuroblastoma and other small round cell tumors by MIETTINEN, M, CHATTEN, J, PAETAU, A, STEVENSON, A

“…Two hundred fifty-five well-characterized formaldehyde-fixed and paraffin-embedded small round cell tumors mainly from children and young adults including 105…”
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Identification of subsets of neuroblastomas by combined histopathologic and N-myc analysis by Shimada, H, Stram, D O, Chatten, J, Joshi, V V, Hachitanda, Y, Brodeur, G M, Lukens, J N, Matthay, K K, Seeger, R C

“…Neuroblastomas show different histopathologic phenotypes, and the tumor cells can carry normal or multiple copies of the N-myc proto-oncogene (MYCN). Studies…”
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Histopathologic prognostic factors in neuroblastic tumors: definition of subtypes of ganglioneuroblastoma and an age-linked classification of neuroblastomas by Shimada, H, Chatten, J, Newton, Jr, W A, Sachs, N, Hamoudi, A B, Chiba, T, Marsden, H B, Misugi, K

“…Histopathologic prognostic factors of 295 pretreatment tumors of a total 641 neuroblastomas and ganglioneuroblastomas were studied with the use of the…”
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Detection of gene fusions in rhabdomyosarcoma by reverse transcriptase-polymerase chain reaction assay of archival samples by Edwards, R H, Chatten, J, Xiong, Q B, Barr, F G

“…Alveolar rhabdomyosarcoma is a pediatric soft-tissue tumor that is often difficult to distinguish from other small round-cell tumors. The PAX3-FKHR and…”
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Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios : Role of the renin-angiotensin system by LACOSTE, Mireille, YI CAI, DANIEL, Laurent, JOUBERT, Madeleine, LAURENT, Nicole, AZIZA, Jacqueline, SELLAMI, Tahya, BEN AMAR, Hatem, JARNET, Catherine, FRANCES, Anne Marie, DAÏKHA-DAHMANE, Farida, COULOMB, Aurore, GUICHARNAUD, Liliane, NEUHAUS, Thomas J, FOLIGUET, Bernard, CHENAL, Pierre, MARCORELLES, Pascale, GASC, Jean Marie, CORVOL, Pierre, GUBLER, Marie Claire, MOUNIER, Francoise, DUMEZ, Yves, BOUVIER, Raymonde, DIJOUD, Frédérique, GONZALES, Marie, CHATTEN, Jane, DELEZOIDE, Anne-Lise

“…Renal tubular dysgenesis is a clinical disorder that is observed in fetuses and characterized by the absence or poor development of proximal tubules, early…”
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Cancer in neonates: the experience at the Children's Hospital of Philadelphia by Gale, G B, D'Angio, G J, Uri, A, Chatten, J, Koop, C E

“…Among 22 neonates treated at the Children's Cancer Research Center of Philadelphia, 11 had neuroblastoma, which in two cases was widely metastatic. There were…”
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Immunohistochemical analysis of Bcl-2, Bcl-X, Mcl-1, and Bax in tumors of central and peripheral nervous system origin by Krajewski, S, Krajewska, M, Ehrmann, J, Sikorska, M, Lach, B, Chatten, J, Reed, JC

“…The expression of Bcl-2, Bcl-X, Mcl-1, and Bax was examined by immunohistochemical methods in 93 tumors of nervous system origin, including 49 gliomas (30…”
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Ossifying tumor of infantile kidney: report of two cases by Chatten, J, Cromie, W J, Duckett, J W

“…Two patients, both male infants, presented with hematuria and were found to have small calcified intrarenal masses interpreted as calculi radiographically…”
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Molecular Assays for Chromosomal Translocations in the Diagnosis of Pediatric Soft Tissue Sarcomas by Barr, Frederic G, Chatten, Jane, D'Cruz, Celina M, Wilson, Albert E, Nauta, Lauren E, Nycum, Lynn M, Biegel, Jaclyn A, Womer, Richard B

“…Objective.—To compare molecular assays for characteristic chromosomal translocations with standard histopathologic and cytogenetic analysis in the differential…”
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Insulin-like growth factor II-mediated proliferation of human neuroblastoma by EL-BADRY, O. M, HELMAN, L. J, CHATTEN, J, STEINBERG, S. M, EVANS, A. E, ISRAEL, M. A

“…Neuroblastoma is an embryonal tumor that typically arises in cells of the developing adrenal medulla. IGF-II mRNA is expressed at high levels in the adrenal…”
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Immunohistochemical evaluation of myeloid leukemia infiltrates (granulocytic sarcomas) in formaldehyde-fixed, paraffin-embedded tissue by Hudock, J, Chatten, J, Miettinen, M

“…Paraffin sections of granulocytic sarcomas (GS) (n = 30) were immunohistochemically evaluated for CD3, CD15 (LeuM1), CD20 (L26), CD31, CD34, CD43, CD45, CD68…”
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Patient-Specific Early Seizure Detection from Scalp EEG by Minasyan, Georgiy R., Chatten, John B., Chatten, Martha Jane, Harner, Richard N.

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Flow cytometric DNA analysis of neuroblastoma. Correlation with histology and clinical outcome by Gansler, T, Chatten, J, Varello, M, Bunin, G R, Atkinson, B

“…Clinical and histologic features of 38 cases of neuroblastoma were compared with data obtained by flow cytometric DNA analysis. Favorable clinical outcome was…”
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Smart Camera-Based Patient-Specific Seizure Detection by Minasyan, Georgiy R., Chatten, Martha Jane, Lindoerfer, Daniel P., Schuman, Adam J., Tyczka, Dale R.

“…Detection of seizures using smart cameras has potential benefits since it does not require contact with the patient and can be easily deployed. Timely seizure…”
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Genetic disorders and major extracardiac anomalies associated with the hypoplastic left heart syndrome by NATOWICZ, M, CHATTEN, J, WEINBERG, P, ZACKAI, E, KELLEY, R. I, CLANCY, R, CONARD, K, GLAUSER, T, HUFF, D, LIN, A, NORWOOD, W, RORKE, L. B, URI, A

“…All pediatric autopsies of patients with hypoplastic left heart syndrome seen during an 11-year interval were reviewed to determine the frequency of underlying…”
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178 Obstructing Nasopharyngeal Epignathi Causing Polyhydramnios by Deems, Daniel A., Poje, Christopher P., Chatten, Jane, Austin, Mitchell B.

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Treatment of children with neurogenic sarcoma. Experience at the Children's Hospital of Philadelphia, 1958-1984 by Raney, B, Schnaufer, L, Ziegler, M, Chatten, J, Littman, P, Jarrett, P

“…Twenty-four children aged 3 months to 18 years (median, 12 years) were treated for neurogenic sarcoma at the Children's Hospital of Philadelphia Cancer…”
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Obstructing nasopharyngeal epignathi causing polyhydramnios by Deems, Daniel A., Poje, Christopher P., Chatten, Jane, Austin, Mitchell B.

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