Results 111 to 120 of about 10,204 (285)

Organoids: development and applications in disease models, drug discovery, precision medicine, and regenerative medicine

open access: yesMedComm, Volume 5, Issue 10, October 2024.
Four main applications of organoids. The main applications of organoids include the construction of disease models, drug screening and toxicity evaluation, precision medicine, and regenerative medicine. Abstract Organoids are miniature, highly accurate representations of organs that capture the structure and unique functions of specific organs ...
Qigu Yao   +6 more
wiley   +1 more source

A case report: retigabine induced oral mucosal dyspigmentation of the hard palate [PDF]

open access: yes, 2015
Background Dyspigmentation of the oral mucosa has a multitude of aetiological causes. Retigabine, a new antiepileptic drug, has the potential side effect of inducing a blue/purple pigmentation of the oral mucosa in addition to the skin, lips, nails and ...
Beacher, Nicholas G.   +2 more
core   +1 more source

Segmental corymbiform congenital melanocytic naevi: Implications for melanocytic embryology

open access: yes
Journal of the European Academy of Dermatology and Venereology, EarlyView.
Nicole Knöpfel   +10 more
wiley   +1 more source

Comprehensive Assessment of Dermatologic and Dysmorphic Manifestations in Patients With Down Syndrome

open access: yesSkin Research and Technology, Volume 30, Issue 10, October 2024.
ABSTRACT Background Down syndrome (DS), a common chromosomal anomaly caused by trisomy of chromosome 21, is characterized by a broad spectrum of phenotypic characteristics across multiple organ systems, including cardiac defects and leukemia. Dermatological findings are prevalent among individuals with DS; however, these issues are frequently ...
Gökhan Kaya, Ceren Alavanda
wiley   +1 more source

Optic disc Edema in patients with fibrous dysplasia/McCune-Albright syndrome: Craniomorphometric analysis and peripapillary retinal nerve fiber layer data

open access: yesData in Brief, 2021
This article reports quantitative measurements of intracranial volume, optic canal area, and peripapillary retinal nerve fiber layer (RNFL) for a cohort of 124 patients with craniofacial fibrous dysplasia/McCune-Albright Syndrome (FD/MAS), previously ...
Layne N. Raborn   +4 more
doaj  

Some aspects of precocious puberty in preschool-age girls [PDF]

open access: yesРМЖ. Мать и дитя, 2022
Yu.Yu. Chebotareva1, Yu.A. Petrov1, M.A. Rodina2 1Rostov State Medical University, Rostov-on-Don, Russian Federation 2Medical Center Sem’ya, Rostov-on-Don, Russian Federation Precocious puberty (PP) remains a challenging issue for pediatrics,
Yu.Yu. Chebotareva   +2 more
doaj  

Denosumab treatment for fibrous dysplasia [PDF]

open access: yes, 2012
Fibrous dysplasia (FD) is a skeletal disease caused by somatic activating mutations of the cyclic adenosine monophosphate (cAMP)‐regulating protein, α‐subunit of the Gs stimulatory protein (G s α).
Albright   +41 more
core   +1 more source

Paediatric thyroid disease

open access: yesClinical Endocrinology, Volume 101, Issue 3, Page 223-233, September 2024.
Abstract The spectrum of thyroid disorders presenting to paediatricians is different to that seen by adult physicians. Referrals reflect cases detected by the neonatal screening programme for congenital hypothyroidism and many of the inherited defects of thyroid hormone generation or action will be manifest in early life. Autoimmune thyroid disease can
Timothy Cheetham, Claire Wood
wiley   +1 more source

Syndrome Measurement Strategies for the [[7,1,3]] Code [PDF]

open access: yesarXiv, 2015
Quantum error correction (QEC) entails the encoding of quantum information into a QEC code space, measuring error syndromes to properly locate and identify errors, and, if necessary, applying a proper recovery operation. Here we compare three syndrome measurement protocols for the [[7,1,3]] QEC code: Shor states, Steane states, and one ancilla qubit by
arxiv  

Treatment of Pathological Bone Fractures in a Patient with McCune-Albright Syndrome

open access: yesCase Reports in Endocrinology, 2013
McCune-Albright syndrome is a rare genetic disorder with typical skeletal and endocrine manifestations. The disease course is complicated by recurrent fractures resulting from polyostotic fibrous dysplasia and the treatment is thus primarily directed at ...
Jana Kollerova   +4 more
doaj   +1 more source

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