Cargando…

Correlation between genetic heterogeneity and variability for response to growth hormone in Noonan syndrome

Detalles Bibliográficos
Autor principal:	Shin, Young-Lim
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Pediatric Society 2019
Materias:	Editorial
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881207/ https://www.ncbi.nlm.nih.gov/pubmed/31319646 http://dx.doi.org/10.3345/kjp.2019.00220

Ejemplares similares

Growth hormone therapy in patients with Noonan syndrome
por: Seo, Go Hun, et al.
Publicado: (2018)

Five-year response to growth hormone in children with Noonan syndrome and growth hormone deficiency
por: Zavras, Niki, et al.
Publicado: (2015)

Response to growth hormone therapy in children with Noonan syndrome: correlation with or without PTPN11 Gene mutation
por: Kim, Yoo-Mi, et al.
Publicado: (2013)

Effectiveness of growth hormone therapy in children with Noonan syndrome
por: Seok, Eun mi, et al.
Publicado: (2020)

Growth, Endocrine Features, and Growth Hormone Treatment in Noonan Syndrome
por: Dahlgren, Jovanna, et al.
Publicado: (2022)

Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome
por: Vurallı, Doğuş, et al.
Publicado: (2016)

Genotypic Findings in Noonan and Non-Noonan RASopathies and Patient Eligibility for Growth Hormone Treatment
por: Carcavilla, Atilano, et al.
Publicado: (2023)

Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height
por: Libraro, Annachiara, et al.
Publicado: (2021)

Effect of Growth Hormone Therapy in Patients with Noonan Syndrome: A Retrospective Study
por: Apperley, Louise Jayne, et al.
Publicado: (2020)

Cardiovascular safety of growth hormone treatment in Noonan syndrome: real-world evidence
por: Romano, Alicia, et al.
Publicado: (2021)

Comparison of effectiveness of growth hormone therapy according to disease-causing genes in children with Noonan syndrome
por: Jo, Kyo Jin, et al.
Publicado: (2019)

Tegumentary manifestations of Noonan and Noonan-related syndromes
por: Quaio, Caio Robledo D'Angioli Costa, et al.
Publicado: (2013)

Noonan syndrome
por: van der Burgt, Ineke
Publicado: (2007)

Etiology and Treatment of Growth Delay in Noonan Syndrome
por: Rodríguez, Fernando, et al.
Publicado: (2021)

Outcomes in growth hormone-treated Noonan syndrome children: impact of PTPN11 mutation status
por: Jorge, Alexander A L, et al.
Publicado: (2022)

Transcriptional Hallmarks of Noonan Syndrome and Noonan-Like Syndrome with Loose Anagen Hair
por: Ferrero, Giovanni Battista, et al.
Publicado: (2012)

Noonan syndrome and related disorders: Alterations in growth and puberty
por: Noonan, Jacqueline A.
Publicado: (2006)

Long-term efficacy of recombinant human growth hormone therapy in short-statured patients with Noonan syndrome
por: Jeong, Insook, et al.
Publicado: (2016)

The Effect of Growth Hormone Therapy on Cardiac Outcomes in Noonan Syndrome: Long Term Follow-up Results
por: Kızılcan Çetin, Sirmen, et al.
Publicado: (2022)

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study
por: Şıklar, Zeynep, et al.
Publicado: (2016)

Clinical manifestations of Noonan syndrome
por: Digilio, MC, et al.
Publicado: (2001)

Recognition Memory in Noonan Syndrome
por: Costanzo, Floriana, et al.
Publicado: (2021)

Development of disease-specific growth charts in Turner syndrome and Noonan syndrome
por: Isojima, Tsuyoshi, et al.
Publicado: (2017)

GH Responsiveness in Children With Noonan Syndrome Compared to Turner Syndrome
por: Dahlgren, Jovanna, et al.
Publicado: (2021)

Personality and Psychopathology in Adults with Noonan Syndrome
por: Roelofs, Renée L., et al.
Publicado: (2019)

The other side of Turner's: Noonan's syndrome
por: Agarwal, Pankaj, et al.
Publicado: (2013)

Noonan syndrome – a new survey
por: Tafazoli, Alireza, et al.
Publicado: (2016)

Noonan syndrome: improving recognition and diagnosis
por: Zenker, Martin, et al.
Publicado: (2022)

Clinical Heterogeneity in two patients with Noonan-like Syndrome associated with the same SHOC2 mutation
por: Capalbo, Donatella, et al.
Publicado: (2012)

The spectrum of genetic variants and phenotypic features of Southeast Asian patients with Noonan syndrome
por: Koh, Ai‐Ling, et al.
Publicado: (2019)

Twin Infant with Lymphatic Dysplasia Diagnosed with Noonan Syndrome by Molecular Genetic Testing
por: Mathur, Deepan, et al.
Publicado: (2014)

LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis
por: Farncombe, Kirsten M., et al.
Publicado: (2022)

Hashimoto thyroiditis with an unusual presentation of cardiac tamponade in Noonan syndrome
por: Lee, Mi Ji, et al.
Publicado: (2016)

Editorial: Endocrine aspects of Noonan syndrome and related syndromes
por: Radetti, Giorgio, et al.
Publicado: (2023)

Pragmatic language impairment in children with Noonan syndrome
por: Selås, Magnhild, et al.
Publicado: (2016)

Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome
por: Miri, Othmane, et al.
Publicado: (2018)

Factor XIII Deficiency Associated With Noonan Syndrome
por: Kharel, Zeni, et al.
Publicado: (2021)

Progressive Left Ventricular Outflow Tract Stenosis in a Noonan Syndrome Patient With Severe Hypertrophic Cardiomyopathy During Growth Hormone Treatment
por: Ichikawa, Yasuhiro, et al.
Publicado: (2022)

A Novel Heterozygous NF1 Variant in a Neurofibromatosis-Noonan Syndrome Patient with Growth Hormone Deficiency: A Case Report
por: Qin, Si, et al.
Publicado: (2023)

Noonan syndrome and Turner syndrome patients respond similarly to 4 years’ growth-hormone therapy: longitudinal analysis of growth-hormone-naïve patients enrolled in the NordiNet® International Outcome Study and the ANSWER Program
por: Lee, Peter A., et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_glq3efr8nmsgihgjs9uea85pq9