Works matching IS 08830738 AND DT 2006 AND VI 21 AND IP 11

Results: 18

Cockayne Syndrome in Adults: Review With Clinical and Pathologic Study of a New Case.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 991, doi. 10.1177/08830738060210110101

By:

Rapin, Isabelle;
Weidenheim, Karen;
Lindenbaum, Yelena;
Rosenbaum, Pearl;
Merchant, Saumil N.;
Krishna, Sindu;
Dickson, Dennis W.

Publication type:

Article

Phenylketonuria in Pediatric Neurology Practice: A Series of 146 Cases.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 987, doi. 10.1177/08830738060210111401

By:

Yalaz, Kalbiye;
Yilmaz, Engin;
Vanli, Lale;
Tokatli, Aysegul;
Anlar, Banu

Publication type:

Article

Recurrent Nocturnal Tongue Biting in a Child With Hereditary Chin Trembling.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 985, doi. 10.1177/08830738060210111101

By:

Goraya, Jatinder S.;
Virdi, Verinderjit;
Parmar, Veena

Publication type:

Article

Mitochondrial DNA Deletion in a Child With Mitochondrial Encephalomyopathy, Growth Hormone Deficiency, and Hypoparathyroidism.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 983, doi. 10.1177/08830738060210111001

By:

Cassandrini, Denise;
Savasta, Salvatore;
Bozzola, Mauro;
Tessa, Alessandra;
Pedemonte, Marina;
Assereto, Stefania;
Stringara, Silvia;
Minetti, Carlo;
Santorelli, Filippo M.;
Bruno, Claudio

Publication type:

Article

Headache as a Sole Manifestation in Nonconvulsive Status Epilepticus.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 981, doi. 10.1177/08830738060210111801

By:

Ghofrani, Mohammad;
Mahvelati, Farhad;
Tonekaboni, Hassan

Publication type:

Article

Novel Mutation Causing Partial Biotinidase Deficiency in a Syrian Boy With Infantile Spasms and Retardation.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 978, doi. 10.1177/08830738060210110301

By:

Mikati, Mohamad A.;
Zalloua, Pierre;
Karam, Pascale;
Zuheir^Habbal, Mohamad;
Rahi, Amal C.

Publication type:

Article

Childhood-Onset Spastic Paraplegia With NIPA1 Gene Mutation.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 974, doi. 10.1177/08830738060210111501

By:

Bien-Willner, Ricardo;
Sambuughin, Nyamkhishig;
Holley, Heather;
odensteiner, John;
Sivakumar, Kumaraswamy

Publication type:

Article

Intravenous Immunoglobulin for Guillain-Barré Syndrome: How Effective?

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 972, doi. 10.1177/08830738060210110701

By:

Ali Tasdemir, Haydar;
Dilber, Cergiz;
Kanvber, Yilmaz;
Uysal, Serap

Publication type:

Article

Novel Mitochondrial DNA Transversion Mutation in Transfer Ribonucleic Acid for Leucine 2 (CUN) in a Patient With the Clinical Features of MELAS.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 971, doi. 10.1177/08830738060210110601

By:

Abu-Amero, Khaled K.;
Ozand, Pinar T.;
Al-Dhalaan, Hesham

Publication type:

Article

Risk Factors for Seizures in Very Low Birthweight Infants With Periventricular Leukomalacia.

Published in:

2006

By:

Kohelet, David;
Shochat, Rina;
Lusky, Ayala;
Reichman, Brian

Publication type:

Bibliography

Exchange Transfusion: A Low-Cost Alternative for Severe Childhood Guillain-Barré Syndrome.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 960, doi. 10.1177/08830738060210111201

By:

Baranwal, Arun K.;
Ravi, Ravi N. M.;
Singh, Rupa

Publication type:

Article

Association of Optic Nerve Hypoplasia With Mitochondrial Cytopathies.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 956, doi. 10.1177/08830738060210111601

By:

Tabn, Mehryar;
Cohen, Bruce H.;
Rothner, A. David;
Traboulsi, Elias I.

Publication type:

Article

Systemic and Ocular Findings in 100 Patients With Optic Nerve Hypoplasia.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 949, doi. 10.1177/08830738060210111701

By:

Garcia, M. Lourdes;
Ty, Edna B.;
Taban, Mehryar;
Rothner, A. David;
Rogers, Douglas;
Traboulsi, Elias I.

Publication type:

Article

Pattern of Childhood Epilepsies With Neuronal Migrational Disorders in Oman.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 945, doi. 10.1177/08830738060210110901

By:

Koul, Roshan;
Jain, Rajeev;
Chacko, Alexander

Publication type:

Article

Behavioral and Emotional Problems in Children With Epilepsy.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 939, doi. 10.1177/08830738060210110501

By:

Frelinger, Michael;
Reisel, Barbara;
Reiter, Edith;
Zelenko, Marina;
Hauser, Erwin;
Seidl, Rainer

Publication type:

Article

Intensive Pediatric Constraint-Induced Therapy for Children With Cerebral Palsy: Randomized, Controlled, Crossover Trial.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 931, doi. 10.1177/08830738060210110401

By:

Deluca, Stephanie C.;
Echols, Karen;
Law, Charles R.;
Ramey, Sharon L.

Publication type:

Article

Lobar Asymmetries in Subtypes of Dyslexic and Control Subjects.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 922, doi. 10.1177/08830738060210110201

By:

Zadina, Janet N.;
Corey, David. M.;
Casbergue, Renee M.;
Lemen, Lisa C.;
Rouse, Jeffrey C.;
Knaus, Tracey A.;
Foundas, Anne L.

Publication type:

Article

Occurrence of and Mortality From Childhood Neuronal Ceroid Lipofuscinoses in Norway.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 917, doi. 10.1177/08830738060210110801

By:

Berit Augestad, Liv;
Dana Flanders, William

Publication type:

Article