Cargando…

Acute Deterioration of Pulmonary Arterial Hypertension (PAH) in a Patient with Neurofibromatosis Type 1 (NF1)

A 56-year-old woman was diagnosed as having chronic obstructive pulmonary disease with heavy smoking. Mild pulmonary hypertension (mean pulmonary arterial pressure: 31 mmHg) was detected at the first visit. She was diagnosed with pulmonary hypertension due to pulmonary disease and medicated only wit...

Descripción completa

Detalles Bibliográficos
Autores principales:	Tanaka, Seiya, Kawahara, Fuko, Miyamoto, Taro, Tsurusaki, Satoshi, Sanuki, Yoshihito, Ozumi, Kiyoshi, Harada, Takashi, Tasaki, Hiromi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2019
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679868/ https://www.ncbi.nlm.nih.gov/pubmed/31428480 http://dx.doi.org/10.1155/2019/2987461

Ejemplares similares

Heart rate recovery is useful for evaluating the recovery of exercise tolerance in patients with heart failure and atrial fibrillation
por: Tanaka, Seiya, et al.
Publicado: (2021)

Complications of Neurofibromatosis 1 (NF1) in an Adult With Multiple Comorbidities
por: Nnomadim, Ozioma P, et al.
Publicado: (2021)

Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma
por: Gutmann, David H., et al.
Publicado: (2013)

A novel neurofibromatosis type 1 (NF1) mutation in a patient with NF1 and pheochromocytoma
por: Seo, Yoorim, et al.
Publicado: (2018)

The Spectrum of NF1 Mutations in Korean Patients with Neurofibromatosis Type 1
por: Jeong, Seon-Yong, et al.
Publicado: (2006)

Cohort profile: life with neurofibromatosis 1 – the Danish NF1 cohort
por: Doser, Karoline, et al.
Publicado: (2022)

The Perceived Influence of Neurofibromatosis Type 1(NF1) on the Parents’ Relationship
por: Wiener, Lori, et al.
Publicado: (2023)

Spinal neurofibromatosis with NF1 mutation in a classic neurofibromatosis type 1 family: A case report and literature review
por: Ning, Zeqian, et al.
Publicado: (2019)

Risk Factors for Bullying Victimization in Children with Neurofibromatosis Type 1 (NF1)
por: Stavinoha, Peter L., et al.
Publicado: (2021)

Impacts of NF1 Gene Mutations and Genetic Modifiers in Neurofibromatosis Type 1
por: Wang, Wei, et al.
Publicado: (2021)

Autism Spectrum Disorder in an Unselected Cohort of Children with Neurofibromatosis Type 1 (NF1)
por: Eijk, S., et al.
Publicado: (2018)

Pathogenic neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq
por: Koster, R., et al.
Publicado: (2021)

Management of spinal deformities and tibial pseudarthrosis in children with neurofibromatosis type 1 (NF-1)
por: Mladenov, Kiril V., et al.
Publicado: (2020)

NFB-17. "Optic Pathway findings in children with Neurofibromatosis type-1 (NF-1)
por: Roka, Kleoniki, et al.
Publicado: (2022)

Neurofibromatosis Type 1 (NF1): Addressing the Transition from Pediatric to Adult Care
por: Radtke, Heather B, et al.
Publicado: (2023)

Mathematical Modeling and Nail Placement Accuracy Analysis of NF-1 Neurofibromatosis Scoliosis
por: Yan, Guangxuan, et al.
Publicado: (2022)

Evaluation of quality of life in adults with neurofibromatosis 1 (NF1) using the Impact of NF1 on Quality Of Life (INF1-QOL) questionnaire
por: Ferner, Rosalie E, et al.
Publicado: (2017)

Accurate Classification of NF1 Gene Variants in 84 Italian Patients with Neurofibromatosis Type 1
por: Stella, Alessandro, et al.
Publicado: (2018)

Can the Cognitive Phenotype in Neurofibromatosis Type 1 (NF1) Be Explained by Neuroimaging? A Review
por: Baudou, Eloïse, et al.
Publicado: (2020)

Correction to: Management of spinal deformities and tibial pseudarthrosis in children with neurofibromatosis type 1 (NF-1)
por: Mladenov, Kiril V., et al.
Publicado: (2021)

Exploring associations between constipation, severity of neurofibromatosis type 1 and NF1 mutational spectrum
por: Ejerskov, Cecilie, et al.
Publicado: (2021)

Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1
por: N. Abdel‐Aziz, Nahla, et al.
Publicado: (2021)

Are neurofibromatosis type 1 (NF1) patients at increased risk of meningioma and in particular malignant meningioma?
por: Evans, D. Gareth R., et al.
Publicado: (2022)

Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?
por: Alkindy, Adila, et al.
Publicado: (2012)

Retracted: Mathematical Modeling and Nail Placement Accuracy Analysis of NF-1 Neurofibromatosis Scoliosis
por: Healthcare Engineering, Journal of
Publicado: (2023)

Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?
por: Santoro, Claudia, et al.
Publicado: (2018)

Deep Intronic LINE-1 Insertions in NF1: Expanding the Spectrum of Neurofibromatosis Type 1-Associated Rearrangements
por: Alesi, Viola, et al.
Publicado: (2023)

Neurofibromatosis Type 1: A Novel NF1 Mutation Associated with Mitochondrial Complex I Deficiency
por: Domingues, Sara, et al.
Publicado: (2014)

Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a Chinese Population
por: Zhang, Jia, et al.
Publicado: (2015)

Clinical characteristics and spectrum of NF1 mutations in 12 unrelated Chinese families with neurofibromatosis type 1
por: Mao, Bin, et al.
Publicado: (2018)

The cell of origin dictates the temporal course of neurofibromatosis-1 (Nf1) low-grade glioma formation
por: Solga, Anne C, et al.
Publicado: (2017)

Isoform-specific NF1 mRNA levels correlate with disease severity in Neurofibromatosis type 1
por: Assunto, Antonia, et al.
Publicado: (2019)

Identification of a Novel NF1 Frameshift Variant in a Chinese Family with Neurofibromatosis Type 1
por: Xu, Guoyao, et al.
Publicado: (2019)

Familial Lipomas Without Classic Neurofibromatosis-1 Caused by a Missense Germline NF1 Mutation
por: Ramirez, Erika, et al.
Publicado: (2021)

Neurofibromatosis 1 with pheochromocytoma
por: Hari Kumar, K. V. S., et al.
Publicado: (2011)

Neurofibromatosis type 1
por: Mançano, Alexandre Dias
Publicado: (2022)

COVID-19 in people with neurofibromatosis 1, neurofibromatosis 2, or schwannomatosis
por: Banerjee, Jineta, et al.
Publicado: (2023)

Targeted exon skipping of NF1 exon 17 as a therapeutic for neurofibromatosis type I
por: Leier, André, et al.
Publicado: (2022)

Recurrent NF1 gene variants and their genotype/phenotype correlations in patients with Neurofibromatosis type I
por: Riva, Matteo, et al.
Publicado: (2021)

Identification of two novel frame shift mutations of the NF1 gene in Korean patients with neurofibromatosis type 1.
por: Park, K. C., et al.
Publicado: (2000)

Cannot write session to /tmp/vufind_sessions/sess_rpbkp516pdqqt1vave4qkn5107