チョレドカルのキストは,あらゆる年齢の人の病気です.

Urinary phenylacetylglutamine (U-PAGN) concentration as biomarker for adherence in patients with urea cycle disorders (UCD) treated with glycerol phenylbutyrate.

Molecular genetics and metabolism reports·2017

Overt hepatic encephalopathy: development of a novel clinician reported outcome tool and electronic caregiver diary.

Metabolic brain disease·2016

Refeeding syndrome in a young woman with argininosuccinate lyase deficiency.

Molecular genetics and metabolism reports·2016

Prospective Multicenter Observational Study of Overt Hepatic Encephalopathy.

Digestive diseases and sciences·2016

Glutamine and hyperammonemic crises in patients with urea cycle disorders.

Molecular genetics and metabolism·2015

Elevated phenylacetic acid levels do not correlate with adverse events in patients with urea cycle disorders or hepatic encephalopathy and can be predicted based on the plasma PAA to PAGN ratio.

Molecular genetics and metabolism·2013

Multivessel coronary artery bypass grafting via small thoracotomy versus sternotomy (MIST): an investigator-initiated, international, open-label, randomised controlled trial.

Lancet (London, England)·2026

Efficacy and safety of once-daily oral zenagamtide, a novel unimolecular GLP-1 and amylin receptor agonist, in adults with type 2 diabetes: a multicentre, randomised, parallel, double-blind, placebo-controlled, dose-finding, phase 2 trial.

Lancet (London, England)·2026

Psoriasis.

Lancet (London, England)·2026

Deramiocel heart-derived cellular therapy in advanced Duchenne muscular dystrophy (HOPE-3): a phase 3, randomised, double-blind, placebo-controlled trial.

Lancet (London, England)·2026

The role of renin, fludrocortisone and hypertension in early childhood in patients with congenital adrenal hyperplasia.

European journal of endocrinology·2026

Real World Outcomes of Metastatic Rhabdomyosarcoma in Children Treated With a Multimodal Protocol: A Single Center Experience.

Journal of pediatric hematology/oncology·2026

Shared Behavioural Determinants of Short Sleep and Obesity From Childhood to Adolescence: An Analyses of Growing Up in Scotland Birth Cohort 1.

Pediatric obesity·2026

A novel CACNA1E mutation (c.1256G > A) was identified in a Chinese patient with epilepsy and congenital heart disease.

Frontiers in medicine·2026

An Evaluation of Community-Based Educational Programming for Prevention of Infant Mortality Among African Americans.

Women's health reports (New Rochelle, N.Y.)·2026

The molecular mechanisms of gas signaling molecules in bronchopulmonary dysplasia related lung injury.

Frontiers in cell and developmental biology·2026

関連する実験動画

チョレドカルのキストは,あらゆる年齢の人の病気です

関連する概念動画

Urinary phenylacetylglutamine (U-PAGN) concentration as biomarker for adherence in patients with urea cycle disorders (UCD) treated with glycerol phenylbutyrate.

Overt hepatic encephalopathy: development of a novel clinician reported outcome tool and electronic caregiver diary.

Refeeding syndrome in a young woman with argininosuccinate lyase deficiency.

Prospective Multicenter Observational Study of Overt Hepatic Encephalopathy.

Glutamine and hyperammonemic crises in patients with urea cycle disorders.

Elevated phenylacetic acid levels do not correlate with adverse events in patients with urea cycle disorders or hepatic encephalopathy and can be predicted based on the plasma PAA to PAGN ratio.

Multivessel coronary artery bypass grafting via small thoracotomy versus sternotomy (MIST): an investigator-initiated, international, open-label, randomised controlled trial.

Efficacy and safety of once-daily oral zenagamtide, a novel unimolecular GLP-1 and amylin receptor agonist, in adults with type 2 diabetes: a multicentre, randomised, parallel, double-blind, placebo-controlled, dose-finding, phase 2 trial.

Psoriasis.

Deramiocel heart-derived cellular therapy in advanced Duchenne muscular dystrophy (HOPE-3): a phase 3, randomised, double-blind, placebo-controlled trial.

The role of renin, fludrocortisone and hypertension in early childhood in patients with congenital adrenal hyperplasia.

Real World Outcomes of Metastatic Rhabdomyosarcoma in Children Treated With a Multimodal Protocol: A Single Center Experience.

Shared Behavioural Determinants of Short Sleep and Obesity From Childhood to Adolescence: An Analyses of Growing Up in Scotland Birth Cohort 1.

A novel CACNA1E mutation (c.1256G > A) was identified in a Chinese patient with epilepsy and congenital heart disease.

An Evaluation of Community-Based Educational Programming for Prevention of Infant Mortality Among African Americans.

The molecular mechanisms of gas signaling molecules in bronchopulmonary dysplasia related lung injury.

関連する実験動画

チョレドカルのキストは,あらゆる年齢の人の病気です

関連する概念動画

関連記事