Results 331 to 340 of about 476,865 (415)

Ununited Fracture of Femur successfully treated by the Seton [PDF]

CHARLES A. POPE
openalex   +1 more source

A comparison of quantitative and semi-quantitative methods for assessing cartilage status and change over time; data from the osteoarthritis initiative. [PDF]

BMC Musculoskelet Disord
Ray A, Brett AD, Dube B, Bowes MA, Rowbotham E, Conaghan PG.   +5 more
europepmc   +1 more source

RETRACTION: The Effect of Two Surgical Modalities for the Treatment of Subtrochanteric Fractures of the Femur on Postoperative Wound Complications in Patients: A Meta-Analysis. [PDF]

Int Wound J
europepmc   +1 more source

Functional morphology of trabecular system in human proximal femur: a perspective from P45 sectional plastination and 3D reconstruction finite element analysis. [PDF]

J Orthop Surg Res
Shah MAA, Lü SJ, Zhang JF, Wang JW, Tang W, Luo WC, Lai HX, Yu SB, Sui HJ.   +8 more
europepmc   +1 more source

THE MANAGEMENT OF FRACTURE OF THE FEMUR

Annals of Surgery, 1930
openaire   +3 more sources

Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2‐Related Disorders to a Syndromic Multiple Tumor Phenotype

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT SETD2 has an essential role in epigenetic regulation. SETD2 pathogenic variants cause neurodevelopmental disorders (SETD2‐NDDs) that most commonly include various degrees of intellectual disability and behavioral disorders, macrocephaly, brain malformations, and generalized overgrowth.
Marie Lucain, Antonio Vitobello, Bekim Sadikovic, Juliette Albuisson, Léa Gaudillat, Martin Chevarin, Julien Maraval, Christel Thauvin‐Robinet, Jennifer Kerkhof, Christophe Philippe, Sophie Nambot, Laurence Faivre   +11 more
wiley   +1 more source

Understanding intra-individual isotopic variability in modern cremated human remains for forensic and archaeological studies. [PDF]

PLoS One
Snoeck C, Beasley MM, Steadman DW.
europepmc   +1 more source

Hereditary Multiple Osteochondromas and Acute Lymphoblastic Leukemia: A Possible Role for EXT1 and EXT2 in Hematopoietic Malignancies

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Hereditary multiple osteochondromas (HMO) is an autosomal dominant disorder caused by heterozygous deleterious variants in the EXT1 or EXT2 genes. While the clinical core phenotype is well established and mainly consists of bone deformities, limb length discrepancies, multiple benign bone neoplasms, and increased risk of chondrosarcoma, the ...
Francesco Comisi, Carmela Fusco, Rosamaria Mura, Carla Cerruto, Leonardo D'Agruma, Salvatore Carnazzo, Marco Castori, Salvatore Savasta   +7 more
wiley   +1 more source

Mandibular-Derived Monocytes from 1-Year-Old Mice Have Enhanced Osteoclast Differentiation and Differentially Regulated Gene Expression Compared to Femur-Derived Monocytes. [PDF]

Biology (Basel)
Asinas ED, Clark R, Nelson J, Llorens JEA, Mansky K, Tasca A.   +5 more
europepmc   +1 more source

A Novel Technique of Hip Disarticulation with a Stump with Soft Tissue of the Proximal Thigh: A Case Report. [PDF]

JBJS Case Connect
Mizuma T, Yamamoto K, Kurihara K, Furusawa K, Kamio S, Hirozane T, Yamaguchi S, Watanabe R, Mori T, Asano N, Nakayama R.   +10 more
europepmc   +1 more source