Results 51 to 60 of about 3,877 (214)

Polimorfismo de deleção de 19 pares de bases do gene dihidrofolato redutase (DHFR): risco materno para síndrome de Down e metabolismo do folato [PDF]

, 2010
CONTEXT AND OBJECTIVE: Polymorphisms in genes involved in folate metabolism may modulate the maternal risk of Down syndrome (DS). This study evaluated the influence of a 19-base pair (bp) deletion polymorphism in intron-1 of the dihydrofolate reductase ...
BISELLI, Joice Matos, CARVALHO, Valdemir Melechco, EBERLIN, Marcos Nogueira, GOLONI-BERTOLLO, Eny Maria, HADDAD, Renato, MENDES, Cristiani Cortez, PAVARINO-BERTELLI, Érika Cristina, RICCIO, Maria Francesca, VANNUCCHI, Hélio, ZAMPIERI, Bruna Lancia   +9 more
core   +1 more source

Computed tomography of the equine caudal spine and pelvis: Technique, image quality and anatomical variation in 56 clinical cases (2018–2023)

Equine Veterinary Journal, Volume 57, Issue 5, Page 1265-1278, September 2025.
Abstract Background Cross‐sectional imaging improves the diagnostic accuracy of complex anatomical regions. Computed tomography (CT) of the pelvis and caudal spine in a large group of live horses and ponies has not been previously reported. Objective To describe the procedure for acquiring CT images of horses' caudal spine/pelvis under general ...
Nadine Kristina Elise Ogden, Katja Winderickx, Alison Bennell, John David Stack   +3 more
wiley   +1 more source

IMPLICATIONS OF PHYSICALTHERAPY REGARDING THE REHABILITATION OF PATIENT WITH SPINA BIFIDA OCCULTA [PDF]

Annals of the “Ştefan cel Mare” University: Physical Education and Sport Section - The Science and Art of Movement, 2018
Today, physicaltherapy requires a wide field of knowledge (anatomy, pathology, psychology, rehabilitation medicine), its applications are common in various diseases of various devices and systems of the body.
Ileana Juravle
doaj  

A Closer Look at the Global Management of Spina Bifida: The Implementation of Endoscopic Third Ventriculostomy in the Treatment of Spina Bifida-Related Hydrocephalus in Africa [PDF]

, 2018
Spina bifida, specifically myelomeningocele, is a debilitating neural tube defect that affects patients and families throughout the world. Traditional management and treatment methods are described, followed by an explanation of why this is often ...
Burckart, Caryssa
core   +1 more source

The effect of a spina bifida-defect at the lumbosacral junction on spinopelvic alignments [PDF]

, 2020
Background: Spina bifida defects, which are mild neurotube defects are commonly found at the lumbosacral junction. The defect which is  associated with micronutrient deficiency (folate) is highly prevalent in impoverished populations; and because ...
Muthuuri, J.M.
core   +1 more source

Neural tube defects [PDF]

, 2014
Neural tube defects (NTDs), including spina bifida and anencephaly, are severe birth defects of the central nervous system that originate during embryonic development when the neural tube fails to close completely.
Copp, AJ, Greene, ND
core   +1 more source

An Enlarging Mass Superimposed on a Giant Congenital Melanocytic Nevus: A Case Report and Review of Literature

Clinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT Congenital melanocytic nevi (CMN), arising from the proliferation of melanocytes, manifest at birth and are colloquially termed as bathing trunk, coat‐sleeve, or stocking nevi. These lesions, occurring in approximately 1 to 2% of neonates, predominantly localize over the trunk and thigh regions.
Nabaa Al‐Zubaidi, Sabertehrani Sayna, Zahra Asadi Kani, Mehdi Gheisari, Khatere Zahedi   +4 more
wiley   +1 more source

Bioarchaeology and burial practices at Capela de Nossa Senhora da Victória (Rio Maior, Portugal) [PDF]

, 2008
A team of archaeologists discovered numerous human remains during three seasons of excavations and architectural analysis at Capela de Nossa Senhora da Victória (Our Lady of Victory Chapel) in Rio Maior, Portugal between 1987 and 1989.
Murphy, Kimmarie, Oliveira, Humberto Nuno de, Pereira, Carlos M. C., Thacker, Paul T., Tucker, Bryan   +4 more
core  

Neurological Evaluation of Severe Congenital Kyphosis With Compressive Myelopathy in 39 Patients With a Minimum 1‐Year Follow‐Up

Orthopaedic Surgery, Volume 17, Issue 7, Page 2004-2014, July 2025.
We suggested that the duration of symptoms and the severity of spinal cord compression were two major contributors to the neurological prognosis in patients with CK. MRI indicators of poor prognosis included the presence of T1WI hypointensity, T2WI hyperintensity, and greater MCC, MSCC, and MTAC.
Jiaqi Zhang, Yan Zeng, Weishi Li
wiley   +1 more source

Weaver Syndrome: A Rare Cause of Neonatal Macrosomia and Dysmorphism. A Case Report. [PDF]

Batna Journal of Medical Sciences
Weaver syndrome is a rare genetic disorder characterized by abnormally excessive growth both in utero and postnatally. It is associated with a mutation in the EZH2 gene, which leads to accelerated bone development and other clinical manifestations such
Fadila BENDAOUD, Hemza GUELLOUH
doaj   +1 more source