Zobrazeno 1 - 10
of 113
pro vyhledávání: '"792"'
Autor:
Kiwako Yamamoto-Hanada
Publikováno v:
The Journal of Pediatrics. 202:330-333
IMPORTANCE: Allergic diseases are prevalent in childhood. Early exposure to medications that can alter the microbiome, including acid-suppressive medications and antibiotics, may influence the likelihood of allergy. OBJECTIVE: To determine whether th
Publikováno v:
Genes
Volume 12
Issue 6
Herlin, M K, Yones, S A, Kjeldsen, E, Holmfeldt, L & Hasle, H 2021, ' What Is Abnormal in Normal Karyotype Acute Myeloid Leukemia in Children? Analysis of the Mutational Landscape and Prognosis of the TARGET-AML Cohort ', Genes, vol. 12, no. 6, 792 . https://doi.org/10.3390/genes12060792
Genes, Vol 12, Iss 792, p 792 (2021)
Volume 12
Issue 6
Herlin, M K, Yones, S A, Kjeldsen, E, Holmfeldt, L & Hasle, H 2021, ' What Is Abnormal in Normal Karyotype Acute Myeloid Leukemia in Children? Analysis of the Mutational Landscape and Prognosis of the TARGET-AML Cohort ', Genes, vol. 12, no. 6, 792 . https://doi.org/10.3390/genes12060792
Genes, Vol 12, Iss 792, p 792 (2021)
Normal karyotype acute myeloid leukemia (NK-AML) constitutes 20–25% of pediatric AML and detailed molecular analysis is essential to unravel the genetic background of this group. Using publicly available sequencing data from the TARGET-AML initiati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a286de8dcad550837546273687e1b1b7
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-449211
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-449211
Autor:
Stéphanie Franchi-Abella, Emmanuel Gonzales, Alexis Galloux, Sophie Branchereau, Erika Pace, Danièle Pariente
Publikováno v:
Pediatric Radiology. 48:667-679
Hepatic venous outflow obstruction after paediatric liver transplantation is an unusual but critical complication. To review the incidence, diagnosis and therapeutic modalities of hepatic venous outflow obstruction from a large national liver transpl
Publikováno v:
JAMA pediatrics. 172(6)
Importance Allergic diseases are prevalent in childhood. Early exposure to medications that can alter the microbiome, including acid-suppressive medications and antibiotics, may influence the likelihood of allergy. Objective To determine whether ther
Autor:
Ayse E, Yilmaz, Guzide, Dogan, Ahmet Z, Akelma, Musemma, Karabel, Duran, Karabel, Halise, Akca, Emire A, Erdur
Publikováno v:
Minerva pediatrica. 68(6)
The aim of this study was to investigate the experiences of Turkish mothers in teething period and the factors affecting teething.This study was performed by filling in questionnaire forms with a face-to-face interview technique with the mothers of 7
Publikováno v:
Nutrition and Health. 28:751-759
Background: Maternal, infant and young child health and nutrition are affected during the COVID-19 pandemic. Aim: This study aimed to present the snapshot situation of maternal health practices of pregnant women including infant and young child feedi
Publikováno v:
Value in Health Regional Issues. 28:14-18
Objectives Nebulized 3% hypertonic solution (HS) is associated with lower total cost and higher quality-adjusted life-years. Nevertheless, the expected budget impact of this drug had not been explicitly estimated. The aim of this study was to evaluat
Autor:
Mohammad Nasyatmuddin Yahya, Bee-See Goh, Fahrin Zara Mohammad Nasseri, Nor Azlin Kamal Nor, Wan Nurulhuda Wan Md Zin, Hasniah Abdul Latif
Publikováno v:
Acta Oto-Laryngologica. 142:187-190
Down syndrome (DS) is the most common human chromosomal genetic disorder; caused by extra copy of chromosome 21-one out of 792 babies globally and one in 950 in Malaysia.To obtain spectrum of upper airway pathology in DS children-prevalence, causes a
Autor:
Madiha Bhatti Söfteland, Peter Tarnow, Sara Fischer, Emma Wikberg, Lars Kölby, Giovanni Maltese
Publikováno v:
Journal of Craniofacial Surgery. 32:2636-2640
In this retrospective study, the authors determined changes in intracranial volume (ICV) and cephalic index (CI) in patients with sagittal craniosynostosis and operated with craniotomy combined with either 2 or 3 springs. The authors included patient
Autor:
H, Khademian, E, Mehravar, Ja, Urtizberea, S, Sagoo, L, Sandoval, R, Carbajo, B, Darvish, Y, Valles-Ayoub, D, Darvish
Publikováno v:
Clinical genetics. 84(6)
GNE myopathy or hereditary inclusion body myopathy (HIBM) is an ultra-rare severely disabling autosomal recessive adult onset muscle disease which affects roughly one to three individuals per million worldwide. Genetically, HIBM is caused by mutation