Results 101 to 110 of about 392,468 (371)

[Characteristic of the fractures of the cervical, thoracic and lumbar vertebrae in the victims of a traffic accident found in the passenger compartment of a modern motor vehicle].

Sudebno-meditsinskaia ekspertiza, 2016
The objective of the present work was to study peculiar features of the injuries to three spinal regions in the victims of a head-on car collision found in the passenger compartments of modern motor vehicles equipped with seat belts and other safety ...
Iu I Pigolkin, I. Dubrovin, E. Sedykh, A. S. Mosoian   +3 more
semanticscholar   +1 more source

Compound Heterozygous Variants in ZSWIM7 Gene Linked to Infertility and Its Role in Gonadal Development

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT This study aims to elucidate the role of the ZSWIM7 gene in the etiology of infertility, focusing on its potential association with premature ovarian insufficiency and azoospermia. We investigated an 18‐year‐old female patient who presented with primary amenorrhea, hypoplasia of the uterus and ovaries, Tanner stage II breast and pubic hair ...
Denise M. Christofolini, Guilherme Pinn, Thainá Vilella, Maria I. Melaragno, Mariana Moysés‐Oliveira, Luciano Pompei, Rare Genomes Project Consortium, Bianca Bianco, Caio P. Barbosa   +8 more
wiley   +1 more source

Laboratory guide to early life history stages of northeast Pacific fishes [PDF]

, 1989
This laboratory guide presents taxonomic information on eggs and larvae of fishes of the Northeast Pacific Ocean (north of California) and the eastern Bering Sea. Included are early-life-history series, illustrations, and comparative descriptions of 232
Blood, Deborah M., Kendall, Jr., Arthur W., Matarese, Ann C., Vinter, Beverly M.   +3 more
core  

Accuracy of transcranial magnetic stimulation and a Bayesian latent class model for diagnosis of spinal cord dysfunction in horses [PDF]

, 2020
Background: Spinal cord dysfunction/compression and ataxia are common in horses. Presumptive diagnosis is most commonly based on neurological examination and cervical radiography, but the interest into the diagnostic value of transcranial magnetic ...
Buczinski, Sebastien, Deprez, Piet, Dumoulin, Michèle, Pardon, Bart, Raes, Els, Rijckaert, Joke, Van Ham, Luc, van Loon, Gunther   +7 more
core   +1 more source

Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
V. Taliercio, J. Zhao, S. E. Boyden, R. Mao, P. Bayrak‐Toydemir, A. Pflaum, J. Palumbos, A. Andrews, E. E. Baldwin, C. Welt, Mackenzie Fait, Undiagnosed Diseases Network, L. D. Botto, D. Viskochil   +13 more
wiley   +1 more source

An Anglo-Saxon execution cemetery at Walkington Wold, Yorkshire [PDF]

, 2007
This paper presents a re-evaluation of a cemetery excavated over 30 years ago at Walkington Wold in east Yorkshire. The cemetery is characterized by careless burial on diverse alignments, and by the fact that most of the skeletons did not have ...
allison k.j., bailey g.b., bartlett j.e., boylston a., briden c., briden c., buikstra j., byers s.n., carver m., daniell c., daniell c., griffith a.f., hadley d.m., hall r.a., hayman g., hill n.g., liddell d.m., meaney a.l., meaney a.l., miles a.e.w., nenk b.s., novak s., pantos a., philpott r., pollard a.m., Reynolds a, reynolds a., reynolds a., richards j.d., rypins s., scheuer l., semple s., skeat w.w., stead i.m., stroud g., suchey j.m., waldron t., west s.e., wymer j.j.   +38 more
core   +1 more source

Ocular Findings as the Most Striking Manifestation of a SMAD3 Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Loeys‐Dietz syndrome (LDS) is a heritable connective tissue disorder with variable expressivity. It is a multisystemic condition mainly characterized by a propensity for arterial aneurysms and dissections, skeletal manifestations, hypertelorism, bifid uvula, craniosynostosis, and cutaneous features.
Noémie Villeneuve‐Cloutier, Christie A Boswell‐Patterson, Lucas Bronicki, Krista M. Vincent, Kalin Wilk, Andrea C. Yu, Gail E. Graham, Julie Richer   +7 more
wiley   +1 more source

MRI and CT findings in anterior thoracic myelomeningocele associated with scoliosis: A case of an 8-year-old child

Radiology Case Reports, 2023
Anterior Thoracic Myelomeningocele is a very rare condition. The diagnosis may be made before or after birth. Association with loss of physiologic curvature of the spine is common.
Patient Aganze Migabo, MD, Abasi Amisi Bulabula, MD, Roméo Murhega Bujiriri, MD, Marius Baguma, PhD, Léon-Emmanuel Mukengeshayi Mubenga, PhD, Ghislain Balemba Maheshe, MD   +5 more
doaj  

Survivorship of Individuals With Double Heterozygosity for Achondroplasia and Type 2 Collagenopathy

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Historically, double heterozygosity, or a diagnosis of two separate, dominant genetic conditions, was often thought to be lethal in individuals with autosomal dominant skeletal dysplasias. In previously published studies of individuals with dual dysplasia diagnoses of achondroplasia and type 2 collagenopathy, infants died of respiratory ...
Valerie R. Schwartz, Andrea Schelhaas, Angela L. Duker, Ricki S. Carroll   +3 more
wiley   +1 more source

VERTEBRAL COLUMN OF MITHUN (Bos frontalis) - ITS BIOMECHANICS IN REFERENCE TO HABITAT ADAPTATION [PDF]

Journal of Veterinary and Animal Sciences, 2018
Vertebral columns of six adult healthy mithun, four male and two female were prepared by simple natural maceration process in water, and then they were cleaned with bleaching powder solution and sun dried.
J.J. Chungath, Malsawm Kima
doaj