Cargando…

Anterior laryngeal membrane and 22q11 deletion syndrome

Detalles Bibliográficos
Autores principales:	Rosa, Rafael Fabiano Machado, Rosa, Rosana Cardoso Manique, Krumenauer, Rita Carolina Pozzer, Varella-Garcia, Marileila, Paskulin, Giorgio Adriano
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2015
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450711/ https://www.ncbi.nlm.nih.gov/pubmed/21860987 http://dx.doi.org/10.1590/S1808-86942011000400024

Ejemplares similares

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

45,X/46,XY mosaicism: report on 14 patients from a Brazilian hospital. A retrospective study
por: Rosa, Rafael Fabiano Machado, et al.
Publicado: (2014)

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

Craniofacial abnormalities among patients with Edwards Syndrome
por: Rosa, Rafael Fabiano M., et al.
Publicado: (2013)

A patient presenting a 22q13 deletion associated with an apparently balanced translocation t(16;22): An illustrative case in the investigation of patients with low ARSA activity
por: Artigalás, Osvaldo, et al.
Publicado: (2012)

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

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects
por: Cirillo, Emilia, et al.
Publicado: (2014)

22q11 deletion syndrome: current perspective
por: Hacıhamdioğlu, Bülent, et al.
Publicado: (2015)

22q11 Deletion Syndrome with Vascular Anomalies
por: Maldjian, Pierre, et al.
Publicado: (2018)

PDGFRA, KIT, and KDR Gene Amplification in Glioblastoma: Heterogeneity and Clinical Significance
por: Carlotto, Bianca Soares, et al.
Publicado: (2023)

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)

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

Detection of 21q11.2‐q22.11 deletions in a fetus by NIPT
por: Zheng, Yunyun, et al.
Publicado: (2019)

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)

A Case of 22q11 Deletion Syndrome (22q11DS) with a Panayiotopoulos Epileptic Pattern: Are Additional Copy-Number Variations a Possible Second Hit in Modulating the 22q11DS Phenotype?
por: Bertini, Veronica, et al.
Publicado: (2017)

A Mini Review on the Contribution of the Anterior Cingulate Cortex in the Risk of Psychosis in 22q11.2 Deletion Syndrome
por: Padula, Maria C., et al.
Publicado: (2018)

Stratification of non-small cell lung cancer patients for therapy with epidermal growth factor receptor inhibitors: the EGFR fluorescence in situ hybridization assay
por: Varella-Garcia, Marileila
Publicado: (2006)

Proton Magnetic Resonance Spectroscopy in 22q11 Deletion Syndrome
por: da Silva Alves, Fabiana, et al.
Publicado: (2011)

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)

22q11.2 Deletion and Duplication Syndromes and COVID-19
por: Crowley, T. Blaine, et al.
Publicado: (2022)

Deletion Syndrome 22q11.2: A Systematic Review
por: Cortés-Martín, Jonathan, et al.
Publicado: (2022)

Clinical management of psychosis in 22q11.2 deletion syndrome
por: Iftimovici, Anton, et al.
Publicado: (2022)

Reproductive Outcomes in Adults with 22q11.2 Deletion Syndrome
por: Palmer, Lisa D., et al.
Publicado: (2022)

Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion
por: PANAGOPOULOS, IOANNIS, et al.
Publicado: (2013)

Efficacy and predictors of success on laryngomalacia surgery: experience from a tertiary pediatric care center in Brazil
por: Drummond, Renata Loss, et al.
Publicado: (2023)

Deletion 22q13.3 syndrome
por: Phelan, Mary C
Publicado: (2008)

The Potential Role of Dysregulated miRNAs in Adolescent Idiopathic Scoliosis and 22q11.2 Deletion Syndrome
por: Montemurro, Nicola, et al.
Publicado: (2022)

Clinical, Immunological, and Genetic Findings in a Cohort of Patients with the DiGeorge Phenotype without 22q11.2 Deletion
por: Alberio, Antonino Maria Quintilio, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_um77qt3c6ri7fbct1jl8qfp631