Results 91 to 100 of about 126,369 (144)

Peer review report 1 on “Hereditary factors are unlikely behind unusual pattern of early - onset colorectal cancer in Egyptians a study of family history and pathology features in Egyptians with large bowel cancer (cross-sectional study)”

, 2017

openalex   +1 more source

Rare severe hereditary maxillary hypoplasia associated with multiple agenesis of the permanent teeth in 2 brothers: A report of 2 cases. [PDF]

Radiol Case Rep
Hariri EM, Idrissi IE, Sellouti M, Ramdi H.   +3 more
europepmc   +1 more source

Addressing uncertainty in hereditary colorectal cancer: the role of a regional expert multidisciplinary team meeting. [PDF]

Fam Cancer
Varde A, McVeigh T, Cuthill V, Brady AF, DeSouza B, Latchford A, Monahan KJ.   +6 more
europepmc   +1 more source

Hereditary Pancreatic Cancer: Advances in Genetic Testing, Early Detection Strategies, and Personalized Management. [PDF]

J Clin Med
Blanco Abad C, Gomila Pons P, Campos Ramírez S, Álvarez Alejandro M, Torres Ramón MI, Miramar Gallart MD, Izquierdo Álvarez S, Polo Marques E, Pazo Cid R.   +8 more
europepmc   +1 more source

Flexibility, Resistance, Aerobic, Movement Execution (FRAME) training program to improve gait capacity in adults with Hereditary Spastic Paraplegia: protocol for a single-cohort feasibility trial. [PDF]

Front Neurol
Boccuni L, Bortolini M, Stefan C, Dal Molin V, Dalla Valle G, Martinuzzi A.   +5 more
europepmc   +1 more source

Costal chondrosarcoma in a woman with hereditary multiple exostoses - a case report. [PDF]

Front Oncol
Yang Z, Wang K, Pu J.
europepmc   +1 more source

A rare case of sporadic metastatic colorectal cancer with glioblastoma multiforme: a challenging clinical scenario. [PDF]

J Surg Case Rep
Awad F, Abdallah F, Alhalabieh A, Aljaafreh I, Naserallah S, Lahham EE.   +5 more
europepmc   +1 more source

The novel SERPINC1 missense mutation c.1148 T > A (p.L383H) causes hereditary antithrombin deficiency and thromboembolism in a Chinese family: a case report. [PDF]

J Med Case Rep
He F, Wang Y, Ning W, Liu C, Guan X, Yao Y.   +5 more
europepmc   +1 more source

Canadian consensus for the assessment and testing of Lynch syndrome. [PDF]

J Med Genet
Aronson M, Palma L, Semotiuk K, Nuk J, Pollett A, Singh H, Rothenmund H, Racher H, Jessen J, Pautler SE, Rusnak A, Rutka M, Etchegary H, Tiano T, Kaurah P, Dawson L, Hawrysh A, Ward T, Bedard A, Sheffield BS, Lerner-Ellis J, Jacob K, Ferguson S, Kim CA, Chamberlain E, Dornan K, Waldman L, Holter S, Horte J, Hyde A, Kwon J, MacMillan A, O'Loughlin M, Tabori U, Gallinger S, Kim R.   +35 more
europepmc   +1 more source

Causative Genes of Homologous Recombination Deficiency (HRD)-Related Breast Cancer and Specific Strategies at Present. [PDF]

Curr Oncol
Nakamura S, Kojima Y, Takeuchi S.
europepmc   +1 more source