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Refinado por: assunto: Medical Sciences remover xxx: xxx remover
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Proconvulsant potential of cyproheptadine in experimental animal models
Proconvulsant potential of cyproheptadine in experimental animal models
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Proconvulsant potential of cyproheptadine in experimental animal models

Singh, Damanpreet ; Goel, Rajesh Kumar

Fundamental & clinical pharmacology, 2010-08, Vol.24 (4), p.451-455 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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Acardia: Epidemiologic findings and literature review from the International Clearinghouse for Birth Defects Surveillance and Research
Acardia: Epidemiologic findings and literature review from the International Clearinghouse for Birth Defects Surveillance and Research
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Acardia: Epidemiologic findings and literature review from the International Clearinghouse for Birth Defects Surveillance and Research

Botto, Lorenzo D. ; Feldkamp, Marcia L. ; Amar, Emmanuelle ; Carey, John C. ; Castilla, Eduardo E. ; Clementi, Maurizio ; Cocchi, Guido ; de Walle, Hermien E.K. ; Halliday, Jane ; Leoncini, Emanuele ; Li, Zhu ; Lowry, R. Brian ; Marengo, Lisa K. ; Martínez-Frías, María-Luisa ; Merlob, Paul ; Morgan, Margery ; Muñoz, Leonora Luna ; Rissmann, Anke ; Ritvanen, Annukka ; Scarano, Gioacchino ; Mastroiacovo, Pierpaolo

American journal of medical genetics. Part C, Seminars in medical genetics, 2011-11, Vol.157C (4), p.262-273

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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3
Clinical Features and Outcomes of Holoprosencephaly in Korea
Clinical Features and Outcomes of Holoprosencephaly in Korea
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Clinical Features and Outcomes of Holoprosencephaly in Korea

Ko, Jung Min, MD ; Kim, Sung Hwan, MD, PhD

Pediatric neurology, 2010-10, Vol.43 (4), p.245-252 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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4
Schizophrenia and Sex Chromosome Anomalies
Schizophrenia and Sex Chromosome Anomalies
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Schizophrenia and Sex Chromosome Anomalies

DeLisi, Lynn E. ; Friedrich, Ursula ; Wahlstrom, Jan ; Boccio-Smith, Angela ; Foreman, Anders ; Eklund, Kurt ; Crow, Timothy J.

Schizophrenia bulletin, 1994, Vol.20 (3), p.495-505 [Periódico revisado por pares]

Oxford: National Institute of Mental Health

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5
Socrates and Temporal Lobe Epilepsy: A Pathographic Diagnosis 2,400 Years Later
Socrates and Temporal Lobe Epilepsy: A Pathographic Diagnosis 2,400 Years Later
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Socrates and Temporal Lobe Epilepsy: A Pathographic Diagnosis 2,400 Years Later

Muramoto, Osamu ; Englert, Walter G.

Epilepsia (Copenhagen), 2006-03, Vol.47 (3), p.652-654 [Periódico revisado por pares]

350 Main Street , Malden , MA 02148 , USA and 9600 Garsington Road , Oxford , OX4 2XG , England: Blackwell Publishing Inc

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6
X inactivation in triploidy and trisomy : the search for autosomal transfactors that choose the active X
X inactivation in triploidy and trisomy : the search for autosomal transfactors that choose the active X
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X inactivation in triploidy and trisomy : the search for autosomal transfactors that choose the active X

MIGEON, Barbara R ; PAPPAS, Kara ; STETTEN, Gail ; TRUNCA, Carolyn ; JACOBS, Patricia A

European journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.153-162 [Periódico revisado por pares]

Avenel, NJ: Nature Publishing

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7
Evidence of zolpidem abuse and dependence: results of the French Centre for Evaluation and Information on Pharmacodependence (CEIP) network survey
Evidence of zolpidem abuse and dependence: results of the French Centre for Evaluation and Information on Pharmacodependence (CEIP) network survey
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Evidence of zolpidem abuse and dependence: results of the French Centre for Evaluation and Information on Pharmacodependence (CEIP) network survey

Victorri‐Vigneau, Caroline ; Dailly, Eric ; Veyrac, Gwenaëlle ; Jolliet, Pascale

British journal of clinical pharmacology, 2007-08, Vol.64 (2), p.198-209 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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8
Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders
Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders
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Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders

Mikhail, Fady M. ; Lose, Edward J. ; Robin, Nathaniel H. ; Descartes, Maria D. ; Rutledge, Katherine D. ; Rutledge, S. Lane ; Korf, Bruce R. ; Carroll, Andrew J.

American journal of medical genetics. Part A, 2011-10, Vol.155A (10), p.2386-2396 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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9
"Not for Human Consumption": A Review of Emerging Designer Drugs
"Not for Human Consumption": A Review of Emerging Designer Drugs
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"Not for Human Consumption": A Review of Emerging Designer Drugs

Musselman, Megan E. ; Hampton, Jeremy P.

Pharmacotherapy, 2014-07, Vol.34 (7), p.745-757 [Periódico revisado por pares]

Boston, MA: Blackwell Publishing Ltd

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10
Outcome of prenatally diagnosed isolated clubfoot
Outcome of prenatally diagnosed isolated clubfoot
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Outcome of prenatally diagnosed isolated clubfoot

Lauson, S. ; Alvarez, C. ; Patel, M. S. ; Langlois, S.

Ultrasound in obstetrics & gynecology, 2010-06, Vol.35 (6), p.708-714 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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