B. L. Maria

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Virginia C Williams, John Lucas, Michael A Babcock, David H Gutmann, Bruce R Korf, B. L. Maria
Pediatrics
2009

Neurofibromatosis type 1 (NF1) is an autosomal dominant condition with a worldwide incidence of approximately 1 per 2500 to 3000 individuals. Caused by a germ-line-inactivating mutation in the NF1… (More)

Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes.

Joseph G Gleeson, Lesley C Keeler, +7 authors William B Dobyns
American journal of medical genetics. Part A
2004

The Molar Tooth Sign (MTS) is defined by an abnormally deep interpeduncular fossa; elongated, thick, and mal-oriented superior cerebellar peduncles; and absent or hypoplastic cerebellar vermis that… (More)

Sturge-Weber syndrome: a review.

Kristin A Thomas-Sohl, Dale F Vaslow, B. L. Maria
Pediatric neurology
2004

Sturge-Weber syndrome is a rare disorder that occurs with a frequency of approximately 1 per 50,000. The disease is characterized by an intracranial vascular anomaly, leptomeningeal angiomatosis,… (More)

"Joubert Syndrome" Revisited: Key Ocular Motor Signs With Magnetic Resonance Imaging Correlation

B. L. Maria, Kim Hoang, +10 authors B Frerking
Journal of child neurology
1997

Joubert syndrome is characterized by episodic hyperpnea and apnea, developmental delay, hypotonia, truncal ataxia, ophthalmologic abnormalities, and vermian dysgenesis. We studied 15 patients with… (More)

Randomized trial of a slow-release versus a standard formulation of cytarabine for the intrathecal treatment of lymphomatous meningitis.

Michael J. Glantz, S LaFollette, +15 authors Stephen B. Howell
Journal of clinical oncology : official journal…
1999

PURPOSE To evaluate the efficacy and safety of a slow-release formulation of cytarabine (DepoCyt; Chiron Corp, Emeryville, CA, and Skye Pharma, Inc, San Diego, CA) that maintains cytotoxic… (More)

Clinical features and revised diagnostic criteria in Joubert syndrome.

B. L. Maria, Eugen Boltshauser, Susan Poveyll Colin N. A. Palmer, Tr X Tran
Journal of child neurology
1999

The clinical presentation of children with Joubert syndrome can include nonspecific features such as hypotonia, ataxia, and developmental delay. Careful examination of the face shows a characteristic… (More)

Molar tooth sign in Joubert syndrome: clinical, radiologic, and pathologic significance.

B. L. Maria, Ronald G. Quisling, +4 authors Emilie Fennell
Journal of child neurology
1999

Joubert syndrome is a rare autosomal-recessive condition characterized by early hyperpnea and apnea, developmental delay, and truncal ataxia. We previously described key ocular motor signs in Joubert… (More)

Hyaluronan, CD44, and emmprin regulate lactate efflux and membrane localization of monocarboxylate transporters in human breast carcinoma cells.

Mark G. Slomiany, George Grass, +4 authors Bryan P. Toole
Cancer research
2009

Interactions of hyaluronan with CD44 in tumor cells play important cooperative roles in various aspects of malignancy and drug resistance. Emmprin (CD147; basigin) is a cell surface glycoprotein of… (More)

Magnetic resonance imaging features and classification of central nervous system malformations in Joubert syndrome.

Ronald G. Quisling, A. James Barkovich, B. L. Maria
Journal of child neurology
1999

This article examines the magnetic resonance imaging features that typify the Joubert malformation. Specific morphologic features include: (1) dysgenesis of the isthmic portion of the brain stem at… (More)

Ependymoma: results, prognostic factors and treatment recommendations.

Mark P. McLaughlin, Robert B. Marcus, +5 authors Rodney R. Million
International journal of radiation oncology…
1998

PURPOSE To review the University of Florida experience in treating ependymomas, analyze prognostic factors, and provide treatment recommendations. METHODS AND MATERIALS Forty-one patients with… (More)

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