Jong Beom Sin

Jong Beom Sin

Department Of Pediatrics, Inje University Busan Paik Hospital, Inje University College Of Medicine, Busan, Korea.

Direct Impact

Concepts for which Jong Beom Sin has direct influence:

preterm infants
pfeiffer syndrome
cutaneous lung tissue heterotopia
poractant alfa
left-sided gastroschisis
multiplex rt-pcr
birth weight

External impact

Concepts related to the work of other authors for which Jong Beom Sin has influence:

pfeiffer syndrome
blood transfusion
seasonal variation
caspofungin therapy
fungal infections
preterm infants
distinct skeletal dysplasia

Prominent publications by Jong Beom Sin

KOL-Index: 27 Systemic fungal infection continues to be a major cause of mortality in extremely low-birth-weight premature infants. Amphotericin B has been recommended as the primary treatment; however, its use is limited due to drug-induced nephrotoxicity and amphotericin B-resistant candidemia. Caspofungin therapy was initiated in seven extremely premature infants at 23 and 24 weeks' gestation with ...
Known for
Persistent Systemic Candidiasis | Extremely Low-Birth-Weight Premature Infants | Liposomal Amphotericin | 23 24 Gestational Age
KOL-Index: 19 Distal duplication, or trisomy 15q, is an extremely rare chromosomal disorder characterized by prenatal and postnatal overgrowth, mental retardation, and craniofacial malformations. Additional abnormalities typically include an unusually short neck, malformations of the fingers and toes, scoliosis and skeletal malformations, genital abnormalities, particularly in affected males, and, in some ...
Known for
Unusually Short Neck | Prenatal Postnatal Overgrowth | Down-Slanting Palpebral Fissures | 42 Clones
KOL-Index: 17 BACKGROUND: Atelosteogenesis type I (AO-I) is a rare lethal skeletal dysplastic disorder characterized by severe short-limbed dwarfism and dislocated hips, knees, and elbows. AO-I is caused by mutations in the filamin B (FLNB) gene; however, several other genes can cause AO-like lethal skeletal dysplasias. METHODS: In order to screen all possible genes associated with AO-like lethal skeletal ...
Known for
Rare Lethal Skeletal Dysplastic | Elbows | Severe Short-Limbed Dwarfism | Flnb
KOL-Index: 16 Pfeiffer syndrome is a rare autosomal dominant disorder characterized by coronal craniosynostosis, brachycephaly, mid-facial hypoplasia, and broad and deviated thumbs and great toes. Pfeiffer syndrome occurs in approximately 1:100,000 live births. Clinical manifestations and molecular genetic testing are important to confirm the diagnosis. Mutations of the fibroblast growth factor receptor 1 ...
Known for
Rare Autosomal Dominant Disorder | Mid-Facial Hypoplasia | C833834gctg Mutation | Gene Fgfr2
KOL-Index: 15 PURPOSE: Anemia of prematurity is frequent in preterm infants, for which red blood cell (RBC) transfusion remains the treatment of choice. In this study, we attempted to evaluate the characteristics and risk factors of anemia of prematurity, and suggest ways to reduce anemia and the need for multiple transfusions. MATERIALS AND METHODS: Preterm infants weighing less than 1500 g (May 2008-May ...
Known for
Hemoglobin Hb Concentration | Phlebotomy | Loss Parenteral | Anemia Birth
KOL-Index: 10 X-linked recessive chondrodysplasia punctata (CDPX1) is a rare congenital disorder of bone and cartilage development, characterized by punctate calcification in areas of endochondral bone formation, leading to stippled epiphyses, severe nasal and midfacial hypoplasia, short stature, and brachytelephalangy. CDPX1 is caused by mutations in the arylsulfatase E (ARSE) gene located on chromosome ...
Known for
Linked Recessive Chondrodysplasia Punctata | Clinically Genetically Confirmed | Cervical Spinal Stenosis | Mutation Arse
KOL-Index: 10 Rotavirus (RV) infection is the primary cause for childhood gastroenteritis worldwide. In Korea, RV infection is most common among children less than 5 years of age. This post-licensure study was conducted to further evaluate the RV vaccine (RIX4414) to provide additional local clinical data to the Korean Food and Drug Association. Healthy infants aged 6-12 weeks were enrolled to receive two ...
Known for
Post-Licensure | Rix4414 Post | Korean Food Drug | Gastroenteritis
KOL-Index: 9 To evaluate two different heel lancet device in terms of pain response and success of the procedure in the preterm infants undergoing heel puncture. 100 preterm infants undergoing capillary blood gas analysis or capillary bilirubin monitoring underwent heel puncture, were randomly allocated to blood sampling from the heel with either a conventional manual lancet or an automatic incision ...
Known for
Procedure Preterm | Bruise | Device Pain | Heel Conventional
KOL-Index: 8 Vitamin D deficiency is still common in pregnant women and infants, especially preterm infants. This study evaluated the prevalence, characteristics, and prenatal and postnatal complications associated with vitamin D deficiency in preterm infants. Preterm infants (gestational age of <32 weeks, delivered between January 2014 and December 2014) were divided into two groups according to ...
Known for
Concentration Hydroxyvitamin | Infants Evaluated | Deficiency Early | Prenatal Complications

Department of Pediatrics, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.

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