Cargando…

Auxological and Endocrinological Features in Children and Adolescents with Cystic Fibrosis

Cystic fibrosis (CF) is a multisystem autosomal recessive disease caused by mutations that lead to deficient or dysfunctional CF transmembrane conductance regulator (CFTR) proteins. Patients typically present malnutrition resulting from the malabsorption of fundamental nutrients and recurring lung i...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ferrari, Vittorio, Terlizzi, Vito, Stagi, Stefano
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9323690/ https://www.ncbi.nlm.nih.gov/pubmed/35887806 http://dx.doi.org/10.3390/jcm11144041

Ejemplares similares

Auxological and endocrinological features in internationally adopted children
por: Stagi, Stefano, et al.
Publicado: (2020)

Auxological and Endocrinological Features in Children With McCune Albright Syndrome: A Review
por: Tufano, Maria, et al.
Publicado: (2020)

Long-term auxological and endocrinological evaluation of patients with 9p trisomy: a focus on the growth hormone-insulin-like growth factor-I axis
por: Stagi, Stefano, et al.
Publicado: (2014)

Auxology – an editorial
por: Hermanussen, Michael, et al.
Publicado: (2014)

Dornase alfa in Cystic Fibrosis: indications, comparative studies and effects on lung clearance index
por: Terlizzi, Vito, et al.
Publicado: (2022)

Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center
por: Casale, Sara, et al.
Publicado: (2023)

Longitudinal Auxological recovery in a cohort of children with Hyperinsulinaemic Hypoglycaemia
por: Worth, Chris, et al.
Publicado: (2020)

Hypertonic saline in people with cystic fibrosis: review of comparative studies and clinical practice
por: Terlizzi, Vito, et al.
Publicado: (2021)

Effect of Dornase Alfa on the Lung Clearance Index in Children with Cystic Fibrosis: A Lesson from a Case Series
por: Terlizzi, Vito, et al.
Publicado: (2022)

Stenotrophomonas maltophilia in people with Cystic Fibrosis: a systematic review of prevalence, risk factors and management
por: Terlizzi, Vito, et al.
Publicado: (2023)

Management and Treatment of Varicocele in Children and Adolescents: An Endocrinologic Perspective
por: Cannarella, Rossella, et al.
Publicado: (2019)

Incidence and evolution of nasal polyps in children and adolescents with cystic fibrosis
por: Weber, Silke Anna Thereza, et al.
Publicado: (2015)

SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators
por: Vannelli, Silvia, et al.
Publicado: (2020)

Effect of Vertebral Fracture on Auxological Profiles of Children Undergoing Acute Lymphoblastic Leukemia Treatment
por: Ahn, Moon Bae, et al.
Publicado: (2021)

Diabetes and Prediabetes in Children With Cystic Fibrosis: A Systematic Review of the Literature and Recommendations of the Italian Society for Pediatric Endocrinology and Diabetes (ISPED)
por: Mozzillo, Enza, et al.
Publicado: (2021)

Proposal of New Auxological Standards for Japanese Girls with Turner Syndrome
por: Isojima, Tsuyoshi, et al.
Publicado: (2010)

Validation of auxological reference values for Japanese children with Noonan syndrome and comparison with growth in children with Turner syndrome
por: Isojima, Tsuyoshi, et al.
Publicado: (2017)

The Relationship between Subnormal Peak-Stimulated Growth Hormone Levels and Auxological Characteristics in Obese Children
por: Barrett, Jefferson, et al.
Publicado: (2014)

Exercise Training in Children and Adolescents with Cystic Fibrosis: Theory into Practice
por: Williams, Craig A., et al.
Publicado: (2010)

Anticipating New Treatments for Cystic Fibrosis: A Global Survey of Researchers
por: Cabral, Bernardo, et al.
Publicado: (2022)

Nocturnal hypoxemia in children and adolescents with cystic fibrosis
por: Ramos, Regina Terse Trindade, et al.
Publicado: (2013)

Cystic Fibrosis: Clinical Phenotypes in Children and Adolescents
por: dos Santos, Ana Luiza Melo, et al.
Publicado: (2018)

Corrigendum to “Validation of auxological reference values for Japanese children with Noonan syndrome and comparison with growth in children with Turner syndrome”
por: Isojima, Tsuyoshi, et al.
Publicado: (2022)

Bone modeling, remodeling, and skeletal health in children and adolescents: mineral accrual, assessment and treatment
por: Maggioli, Chiara, et al.
Publicado: (2017)

Management Issues for Adolescents with Cystic Fibrosis
por: Withers, Adelaide Lindsay
Publicado: (2012)

Comparison between Gibson–Cooke and Macroduct Methods in the Cystic Fibrosis Neonatal Screening Program and in Subjects Who Are Cystic Fibrosis Screen-Positive with an Inconclusive Diagnosis
por: Dolce, Daniela, et al.
Publicado: (2023)

Clinical and Genotypical Features of False-Negative Patients in 26 Years of Cystic Fibrosis Neonatal Screening in Tuscany, Italy
por: Taccetti, Giovanni, et al.
Publicado: (2020)

Sleep Respiratory Disorders in Children and Adolescents with Cystic Fibrosis and Primary Ciliary Dyskinesia
por: Papale, Maria, et al.
Publicado: (2023)

Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review
por: Terlizzi, Vito, et al.
Publicado: (2022)

Endocrinological Involvement in Children and Adolescents Affected by COVID-19: A Narrative Review
por: Calcaterra, Valeria, et al.
Publicado: (2023)

Multidrug-Resistant Bacteria in Children and Adolescents with Cystic Fibrosis
por: Fainardi, Valentina, et al.
Publicado: (2022)

Nasal endoscopic evaluation of children and adolescents with cystic fibrosis
por: Paiva Franco, Letícia, et al.
Publicado: (2015)

Clinical course and endocrinological characteristics of prolactinoma in children and adolescents
por: Kim, Yoo-Mi, et al.
Publicado: (2013)

Constitutional Delay Influences the Auxological Response to Growth Hormone Treatment in Children with Short Stature and Growth Hormone Sufficiency
por: Gunn, Katherine C., et al.
Publicado: (2014)

Nutritional Care in Children with Cystic Fibrosis
por: Mariotti Zani, Elena, et al.
Publicado: (2023)

Auxo-Endocrinological Approach to Celiac Children
por: Bozzola, Mauro, et al.
Publicado: (2015)

Functional Endocrinology from Birth through Adolescence
por: Bondy, P. K.
Publicado: (1953)

Modulator Therapy in Cystic Fibrosis Patients with cis Variants in F508del Complex Allele: A Short-Term Observational Case Series
por: Terlizzi, Vito, et al.
Publicado: (2022)

The “Fortilat” Randomized Clinical Trial Follow-Up: Auxological Outcome at 18 Months of Age
por: Peila, Chiara, et al.
Publicado: (2020)

G378X‐I148T CFTR variant: A new complex allele in a cystic fibrosis newborn with pancreatic insufficiency
por: Terlizzi, Vito, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_0b4tru2ki6718ugfabj1aspeed