๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Incidence and clinical characteristics of hereditary disorders associated with venous thrombosis

โœ Scribed by Dr. Maria Dolores Tabernero; Jose Francisco Tomas; Ignacio Alberca; Alberto Orfao; Antonio Lopez Borrasca; Vicente Vicente

Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
553 KB
Volume
36
Category
Article
ISSN
0361-8609

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Prevalence of hereditary thrombophilia i
Prevalence of hereditary thrombophilia in patients with thrombosis in different venous systems
โœ Thomas Bombeli; Adila Basic; Joerg Fehr ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 77 KB ๐Ÿ‘ 2 views

The prevalence of hereditary thrombophilia is well known in patients with lower-extremity thrombosis but only poorly studied in patients with thrombosis at unusual sites. Consequently, it is still unclear whether such patients should generally be screened for hereditary thrombophilia. We retrospecti

Superficial venous thrombosis associated
Superficial venous thrombosis associated with congenital absence of the inferior vena cava and previous episode of deep venous thrombosis
โœ Darren M. Evanchuk; Ann Von Gehr; James L. Zehnder ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 129 KB ๐Ÿ‘ 2 views

## Abstract Congenital malformations of the inferior vena cava (IVC) are uncommon and may be associated with an increased risk of venous thrombosis. We report the case of a man with congenital absence of the IVC and remote history of deep venous thrombosis who now presents with severe abdominal wal

Genetic associations with clinical chara
Genetic associations with clinical characteristics in bipolar affective disorder and recurrent unipolar depressive disorder
โœ Ho, Luk W.; Furlong, Robert A.; Rubinsztein, Judy S.; Walsh, Cathy; Paykel, Euge ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 30 KB ๐Ÿ‘ 2 views

Genetic factors may be associated with disease subtype as well as susceptibility. We have therefore typed polymorphisms at the serotonin transporter, dopamine receptor, tryptophan hydroxylase, tyrosine hydoxylase, and monoamine oxidase A (MAOA) loci in 139 unipolar and 131 bipolar patients and inves

Clinical report of three patients with h
Clinical report of three patients with hereditary hemochromatosis and movement disorders
โœ G. Demarquay; A. Setiey; Y. Morel; C. Trepo; G. Chazot; E. Broussolle ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 40 KB ๐Ÿ‘ 1 views

Neurologic manifestations are rarely described in hereditary hemochromatosis (HH). We describe three patients with HH and movement disorders. Patient 1, a 69-year-old man, had a 13-year history of disabling cerebellar syndrome, action tremor and myoclonus, and secondary dementia. Patient 2 was a 40-