Cargando…

Erratum to: Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome

Detalles Bibliográficos
Autores principales:	Kim, Eun-Hee, Yum, Mi-Sun, Lee, Beom-Hee, Kim, Hyo-Won, Lee, Hyun-Jeoung, Kim, Gu-Hwan, Lee, Yun-Jeong, Yoo, Han-Wook, Ko, Tae-Sung
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Neurological Association 2016
Materias:	Erratum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828578/ https://www.ncbi.nlm.nih.gov/pubmed/27074298 http://dx.doi.org/10.3988/jcn.2016.12.2.251

Ejemplares similares

Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome
por: Kim, Eun-Hee, et al.
Publicado: (2016)

Psychotic Features as the First Manifestation of 22q11.2 Deletion Syndrome
por: Kook, So Dahm, et al.
Publicado: (2010)

Various Psychiatric Manifestation in DiGeorge Syndrome (22q11.2 Deletion Syndrome): A Case Report
por: Kim, Giok, et al.
Publicado: (2020)

Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndrome
por: AlKalaf, Heeba Y., et al.
Publicado: (2020)

Delayed Diagnosis of Chromosome 22q11.2 Deletion Syndrome Due to Late-Onset Generalized Epilepsy
por: Lee, Seon-Kyung, et al.
Publicado: (2020)

Erratum to “Partial Gene Deletions of PMP22 Causing Hereditary Neuropathy with Liability to Pressure Palsies”
por: Cho, Sun-Mi, et al.
Publicado: (2015)

Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome
por: Maynard, Thomas M, et al.
Publicado: (2020)

Erratum to: 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening
por: Wenger, Tara L., et al.
Publicado: (2016)

Erratum to: Neural correlates of reward processing in adults with 22q11 deletion syndrome
por: Van Duin, Esther D. A., et al.
Publicado: (2016)

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders
por: Jalal, Rhideeta, et al.
Publicado: (2021)

The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS)()
por: van den Bree, Marianne B.M., et al.
Publicado: (2013)

Important Consideration in Choosing Antipsychotics in the Treatment of Patients with 22q11.2 Deletion Syndrome: Risk of Convulsion
por: Choi, Seo-Hyun, et al.
Publicado: (2020)

Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
por: Heung, Tracy, et al.
Publicado: (2022)

Two Cases of Chromosome 22q11.2 Deletion Syndrome Diagnosed in 12-Year-Old Boys with Hypocalcemic Seizures
por: Hyun, Jae Won, et al.
Publicado: (2012)

Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome
por: Lee, Mi-Young, et al.
Publicado: (2014)

Erratum: Effects of Cannabidiol on Adaptive Behavior and Quality of Life in Pediatric Patients With Treatment-Resistant Epilepsy
por: Kim, Se Hee, et al.
Publicado: (2023)

Erratum: Comparison between Clinical Disabilities and Electrophysiological Values in Charcot-Marie-Tooth 1A Patients with PMP22 Duplication
por: Kim, Young Hwa, et al.
Publicado: (2012)

Erratum
por: Yim, Jisook, et al.
Publicado: (2015)

Case Report: Ménière's Disease-Like Symptoms in 22q11.2 Deletion Syndrome
por: Choi, Kwang-Dong, et al.
Publicado: (2021)

Hematological abnormalities and 22q11.2 deletion syndrome
por: Rosa, Rafael Fabiano Machado, et al.
Publicado: (2011)

Obesity in adults with 22q11.2 deletion syndrome
por: Voll, S, et al.
Publicado: (2016)

Risk of malignancy in 22q11.2 deletion syndrome
por: Stevens, Toer, et al.
Publicado: (2017)

The Genetics and Epigenetics of 22q11.2 Deletion Syndrome
por: Du, Qiumei, et al.
Publicado: (2020)

Complement Activation in 22q11.2 Deletion Syndrome
por: Grinde, Dina, et al.
Publicado: (2020)

Laryngeal web with 22q11.2 deletion syndrome
por: Abe, Yasuhiro, et al.
Publicado: (2022)

Tonsillectomy in Children with 22q11.2 Deletion Syndrome
por: Arganbright, Jill M., et al.
Publicado: (2022)

Endocrine and Growth Disorders in Taiwanese Children With 22q11.2 Deletion Syndrome
por: Lin, Han-Yi, et al.
Publicado: (2022)

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
por: Schonherz, Yael, et al.
Publicado: (2014)

Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome)
por: Digilio, MC, et al.
Publicado: (2005)

ERRATUM: Ketogenic Diet for Children with Epilepsy: A Practical Meal Plan in a Hospital
por: Lee, Eunjoo, et al.
Publicado: (2016)

Evaluation of 22q11.2 deletion in Cleft Palate patients
por: Prabodha, L. B. Lahiru, et al.
Publicado: (2012)

Genotype-phenotype correlation in 22q11.2 deletion syndrome
por: Michaelovsky, Elena, et al.
Publicado: (2012)

Psychopathology and cognition in children with 22q11.2 deletion syndrome
por: Niarchou, Maria, et al.
Publicado: (2014)

Otologic and audiologic findings in 22q11.2 deletion syndrome
por: Verheij, E., et al.
Publicado: (2016)

Psychiatric Disorders Associated with 22q11.2 Deletion Syndrome
por: Gambini, Orsola
Publicado: (2016)

Disrupted anatomic networks in the 22q11.2 deletion syndrome
por: Schmitt, J. Eric, et al.
Publicado: (2016)

Visual processing deficits in 22q11.2 Deletion Syndrome
por: Biria, Marjan, et al.
Publicado: (2017)

Clinical variability of chromosome 22q11.2 deletion syndrome
por: Boyarchuk, Oksana, et al.
Publicado: (2017)

22q11.2 Deletion Syndrome–Associated Parkinson's Disease
por: Boot, Erik, et al.
Publicado: (2018)

Dopaminergic neurons in chromosome 22q11.2 deletion syndrome
por: Inoue, Haruhisa
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_s2mh17m06vp83mbv7son2tifgm