Farmacogenética en Fibrosis Quística. [PDF]
, 2017 La fibrosis quística (a partir de ahora referida como FQ) fue descrita por primera vez en 1936 como una entidad separada. También recibía el nombre de “mucoviscidosis” debido a la acumulación de espesas secreciones mucosas que bloqueaban las vías aéreas,
Oraá Pérez, Javier
core
Polysaccharides and mucin 5AC (MUC5AC) expression in gallbladder mucosa of young patients with gallstones as evaluated by spatial visualization and quantification [PDF]
, 2010 The study aimed at examination of tissue expression of polysaccharides and secretory mucin 5AC (MUC5AC)in young patients (up to 25 years of age) with a symptomatic gallstones.
Agnieszka Adamek +6 more
core +2 more sources
Stigma and cystic fibrosis Estigma y fibrosis cística Estigma e fibrose c��stica
Revista Latino-Americana de Enfermagem, 2010 Cystic Fibrosis (CF), also known as Mucoviscidosis, is a chronic disease of autosomal recessive origin and so far incurable. This analysis considers some characteristics of patients and family members that indicate it is a stigmatizing disease.
Tainá Maues Peluci Pizzignacco +2 more
doaj +1 more source
Consequences of cystic fibrosis transmembrane regulator mutations on inflammatory cells [PDF]
, 2016 Recent studies in cystic fibrosis (CF) transmembrane regulator (CFTR) mutations and function have shed light on its involvement in disease progression. The extent of cell and tissue distribution of CFTR facilitates systemic dysfunction of ion transport ...
Castro, Guillermo Raul +2 more
core +1 more source
Sleep habits and pattern in 1-14 years old children and relationship with video devices use and evening and night child activities [PDF]
, 2017 Background: Sleep in childhood and adolescence is crucial for mental and physical health; however several researches reported an increasing trend towards a sleep deprivation in this age. Due to the lack of recent epidemiological studies in Italy, the aim
Bernasconi, Sergio +15 more
core +1 more source
Microbes Saving Lives and Reducing Suffering
Microbial Biotechnology, Volume 18, Issue 1, January 2025.
Kenneth Timmis +26 more
wiley +1 more source
Predictive Factors of Abdominal Compartment Syndrome in Neonatal Age [PDF]
, 2014 In the pediatric population, abdominal compartment syndrome (ACS) is a known complication of abdominal wall defect repair. However, there are only few reports on ACS in newborns and only a proposal of critical intra-abdominal pressure value (IAP) in term
Corsello, G. +7 more
core +1 more source
Safety, Tolerability, and Effects of Sodium Bicarbonate Inhalation in Cystic Fibrosis. [PDF]
, 2020 BACKGROUND:Among the many consequences of loss of CFTR protein function, a significant reduction of the secretion of bicarbonate (HCO3-) in cystic fibrosis (CF) is a major pathogenic feature.
Clinckspoor, Karl Jan +12 more
core +1 more source
Mental disorders in patients with cystic fibrosis
KlinicistIntroduction. Cystic fibrosis (CF) is a genetic disease that leads to dysfunction of internal organs and significantly increases the risk of respiratory infections. According to the N. P.
A. A. Klimenko, A. Yu. Aleksandrova
doaj +1 more source
Learning from each other: ABC transporter regulation by protein phosphorylation in plant and mammalian systems [PDF]
, 2015 The ABC (ATP-binding cassette) transporter family in higher plants is highly expanded compared with those of mammalians. Moreover, some members of the plant ABCB subfamily display very high substrate specificity compared with their mammalian ...
Aryal, Bibek +2 more
core +1 more source