Results 41 to 50 of about 5,717,926 (305)

Identification of misconceptions in the teaching of biology

open access: yes, 2015
peer ...
Galvin, E.   +2 more
openaire   +1 more source

Solid Pseudopapillary Neoplasm of the Pancreas in Children and Adolescents: Expert Recommendations

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Solid pseudopapillary neoplasm of the pancreas (SPN) is a rare low‐grade malignant exocrine pancreatic tumor, mostly discovered during the second decade of life in females, with a very good prognosis, provided microscopically complete surgical excision is achieved.
Sabine Irtan   +18 more
wiley   +1 more source

Ovarian Sex Cord Stromal Tumors in Children and Adolescents—The European Standard Clinical Practice Recommendations

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT As part of the European Cooperative Study Group for Paediatric Rare Tumours initiative, we developed standard clinical practice guidelines for ovarian sex cord stromal tumors, based on comprehensive national and international cohort analyses, literature review, and a final expert consensus conference.
Dominik T. Schneider   +15 more
wiley   +1 more source

Ultrasonographic and Three-Dimensional Analyses at the Glabella and Radix of the Nose for Botulinum Neurotoxin Injection Procedures into the Procerus Muscle

open access: yesToxins, 2019
Botulinum neurotoxin (BoNT) injections are widely used for facial rejuvenation procedures, and the procerus muscle is a major target in cases of glabellar transverse lines or rhytids.
Younghoon Cho   +5 more
doaj   +1 more source

Identification of longevity genes with systems biology approaches

open access: yesAdvances and Applications in Bioinformatics and Chemistry, 2009
Identification of genes involved in the aging process is critical for understanding the mechanisms of age-dependent diseases such as cancer and diabetes. Measuring the mutant gene lifespan, each missing one gene, is traditionally employed to identify longevity genes.
Yuanyou, Tan   +3 more
openaire   +3 more sources

Evidence‐Informed Multidisciplinary Consensus Guidance for the Psychosocial Care of Adolescents With High‐Risk Cancer: Recommendations From the Italian Association of Pediatric Hematology and Oncology

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Adolescents with high‐risk cancer face complex developmental, psychosocial, and ethical challenges that extend beyond disease‐directed treatment. Although international recommendations exist for communication, psychosocial care, pediatric palliative care, survivorship, and shared decision‐making, these have largely evolved within ...
Johanna M. C. Blom   +15 more
wiley   +1 more source

Acknowledgement to Reviewers of Biology in 2014

open access: yes, 2015
The editors of Biology would like to express their sincere gratitude to the following reviewers for assessing manuscripts in 2014:[...
Biology Editorial Office
core   +1 more source

Identification of Functional Modules That Correlate with Phenotypic Difference: The Influence of Network Topology [PDF]

open access: yes, 2010
A gene set enrichment analysis method for including network topology in the identification of genes involved in phenotypic alterations is described. One of the important challenges to post-genomic biology is relating observed phenotypic alterations to ...
Jui-Hung Hung   +11 more
core   +1 more source

Early Body Mass Index z‐Score Change and Resolution of Severe Malnutrition in Children With Sickle Cell Anemia in a Low‐Income Setting: A Prospective Single‐Arm Extension Study

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Children with sickle cell anemia (SCA) in low‐income settings are at risk of severe malnutrition, but optimal nutritional management has not been established. We evaluated an intensified ready‐to‐use therapeutic food (RUTF) regimen in children with persistent severe malnutrition after initial treatment and assessed whether early ...
Safiya Gambo   +9 more
wiley   +1 more source

Whole-exome sequencing revealed a novel heterozygous variant of NF1 in a Vietnamese family with neurofibromatosis type I

open access: yesEgyptian Journal of Medical Human Genetics
Background Neurofibromatosis type I (NF1) is one of the most common autosomal dominant disorders caused by mutations in the NF1 gene. Pathogenic variants in this gene induce a wide range of phenotypes, including dermal neurofibromas along nerves ...
Thao Huong Dinh   +3 more
doaj   +1 more source

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