Results 231 to 240 of about 727,838 (288)

Hereditary gynecological cancer management in women with Lynch syndrome: a survey across Europe. [PDF]

open access: yesFam Cancer
Kwinten KJJ   +4 more
europepmc   +1 more source

Pittsburgh compound B positron emission tomography detects cardiomyopathy in hereditary transthyretin amyloidosis patients with negative bone scintigraphy: a pilot study. [PDF]

open access: yesFront Nucl Med
Tingen HSA   +10 more
europepmc   +1 more source

Clinical and genetic diagnostic challenges in presumed hereditary ataxia. [PDF]

open access: yesJ Neurol
Faust H   +9 more
europepmc   +1 more source

Hereditary ovarian cancer. [PDF]

open access: yesDiscov Oncol
Jurgiel WA, Panasiuk B, Posmyk R.
europepmc   +1 more source

Therapeutic Efficacy and Safety Profile of Eplontersen in Hereditary Transthyretin-Mediated Amyloidosis: A Systematic Review. [PDF]

open access: yesHealth Sci Rep
Patel ZV   +8 more
europepmc   +1 more source
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Hereditary Cancer

Acta Oncologica, 1999
Cancer cases are often clustered in certain families and pedigree analysis indicates that at least 5% of cancer patients have a genetic predisposition to the disease. During the past decade the basic mechanisms for hereditary cancer have been outlined and a large number of the genes involved have been identified.
A, Lindblom, M, Nordenskjöld
openaire   +2 more sources

Hereditary neuropathy

2023
The hereditary neuropathies, collectively referred as Charcot-Marie-Tooth disease (CMT) and related disorders, are heterogeneous genetic peripheral nerve disorders that collectively comprise the commonest inherited neurological disease with an estimated prevalence of 1:2500 individuals. The field of hereditary neuropathies has made significant progress
Chiara, Pisciotta, Michael E, Shy
openaire   +2 more sources

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