human | Q5 |
P6178 | Dimensions author ID | 0775156134.40 |
P496 | ORCID iD | 0000-0001-8012-5433 |
P106 | occupation | researcher | Q1650915 |
Q36809799 | A long-Segmental Vascular Malformation in the Small Bowel Presenting With Gastrointestinal Bleeding in a Preschool-Aged Child |
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Q33918248 | Clinical Characteristics and Ultrasonographic Findings of Acute Bacterial Enterocolitis in Children. |
Q37561069 | Clinical Characteristics of Failure to Thrive in Infant and Toddler: Organic vs. Nonorganic |
Q90254897 | Comparison of effectiveness of growth hormone therapy according to disease-causing genes in children with Noonan syndrome |
Q90469930 | Comparison of four nutritional screening tools for Korean hospitalized children |
Q37627692 | Cytogenetic prognostication within medulloblastoma subgroups |
Q37073617 | Divergent clonal selection dominates medulloblastoma at recurrence |
Q40065199 | Epidemiological Correlation between Fecal Adenovirus Subgroups and Pediatric Intussusception in Korea |
Q53130845 | Esophageal adenocarcinoma and Barrett esophagus in a neurologically impaired teenager. |
Q33935181 | Fundoplication in neonates and infants with primary gastroesophageal reflux |
Q38439221 | Identification of KMT2D and KDM6A mutations by exome sequencing in Korean patients with Kabuki syndrome. |
Q38671456 | Intertumoral Heterogeneity within Medulloblastoma Subgroups |
Q55516275 | Management of Pediatric Patients Presenting with Acute Abdomen Accompanying Dilatation of the Common Bile Duct. |
Q91849443 | Medication-Related Knowledge and Medication Adherence in Pediatric and Adolescent Patients with Inflammatory Bowel Disease |
Q53260096 | NEU1 mutation in a Korean infant with type 2 sialidosis presenting as isolated fetal ascites. |
Q92982538 | Newly Diagnosed Klippel-Trenaunay Syndrome Presenting with Rectal Polyposis in a Male Pediatric Patient: A Case Report |
Q55013618 | Nutritional Screening Tools among Hospitalized Children: from Past and to Present. |
Q98191465 | Pattern of Relapse and Treatment Response in WNT-Activated Medulloblastoma |
Q37004219 | Prognostic value of medulloblastoma extent of resection after accounting for molecular subgroup: a retrospective integrated clinical and molecular analysis |
Q92247505 | The Most Common Cause of Lower Gastrointestinal Bleeding without Other Symptoms in Children is Colonic Polyp: Is Total Colonoscopy Needed? |
Q53283990 | The PRSS1 c.623G>C (p.G208A) mutation is the most common PRSS1 mutation in Korean children with hereditary pancreatitis. |
Q37130238 | Therapeutic Impact of Cytoreductive Surgery and Irradiation of Posterior Fossa Ependymoma in the Molecular Era: A Retrospective Multicohort Analysis |
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