Results 11 to 20 of about 24,775,971 (291)

Thrombosis in Brothers With Protein S Deficiency: Case Series [PDF]

Clinical Case Reports
Hereditary protein S deficiency is a rare thrombophilia that increases the risk of venous thromboembolism (VTE), including thrombosis in unusual sites.
Abate Bane Shewaye, Seifu Kebede, Amsalework Daniel, Kaleb Assefa Berhane, Asteraye Tsige Minyilshewa, Besufikad Girma Kebede   +5 more
doaj   +2 more sources

Livedoid vasculopathy in protein S deficiency [PDF]

Pan African Medical Journal
A 38-year-old female patient presented to the General Medicine Outpatient Department (OPD) with chief complaints of multiple ulcerations associated with pain over the bilateral lower limbs which was present for 1 month. The patient had initially taken only symptomatic treatment with a topical steroid preparation prescribed by a general practitioner but
Hemant Juneja, Gaurang Aurangabadkar
openaire   +4 more sources

Clot In Transit in a Patient with Protein S Deficiency [PDF]

European Journal of Case Reports in Internal Medicine, 2022
Clot in transit (CIT) is a rare condition in which a venous thromboembolism becomes lodged in the right heart. It is seen in up to 18% of patients with massive pulmonary embolism, and if left untreated, mortality rates are between 80% and 100%.
Simon Kashfi, Mohamed Farhan Nasser, Aron Soleiman, Sapna Sharma, Venkata Sandeep Koripalli, Shorabh Sharma   +5 more
doaj   +2 more sources

Thrombosis-related characteristics of pregnant women with antithrombin deficiency, protein C deficiency and protein S deficiency in Japan [PDF]

Thrombosis Journal
Background  We previously conducted a primary survey of pregnant women with hereditary thrombophilia based on national surveillance in Japan, but did not examine their thrombosis-related characteristics.
Takao Kobayashi, Kazuko Sugiura, Toshiyuki Ojima, Mariko Serizawa, Kyuya Hirai, Eriko Morishita   +5 more
doaj   +2 more sources

Acute Reversal of Warfarin Therapy in Patient with Protein C and S Deficiency Presenting for Emergency Surgery [PDF]

The Indian Anaesthetists' Forum, 2010
This is a case report of a 19 year young male presented with swelling and blackening of right upper limb and abdominal pain since 10 days. He was a known case of protein C and protein S deficiency on warfarin therapy, with deranged coagulation parameters
Sananta kumar Dash, Harshel G Parikh, Saurabh B Tiwari, Bharti D Kondwilkar   +3 more
doaj   +2 more sources

Protein S deficiency manifesting with cerebral arterial and venous thrombosis in a young female with kissing carotids phenomenon [PDF]

Thrombosis Journal
Background Majority of people with “kissing carotids”, an anatomical variation of the cervical carotid arteries showing tortuosity, kinking or coiling and coming in proximity at the midline are asymptomatic.
Salvatore Ssemmanda
doaj   +2 more sources

A rare case of autoimmune hemolytic anemia with protein S deficiency with splenic infarct [PDF]

Asian Journal of Transfusion Science
Splenic infarction is a rare entity in pediatric population and is associated with predisposing conditions, i.e., hematological and oncological or infections.
Afreen Khan, Twisha Ishani, Ishaq Farooq, Devki Nandan, Shohrab Alam   +4 more
doaj   +2 more sources

ISOLATED PROTEIN S DEFICIENCY [PDF]

Australasian Medical Journal, 2012
Isolated protein S deficiency is an inherited condition having proven association with venous thromboembolism. There is controversy regarding clear association between protein S deficiency and arterial thrombosis. It is therefore necessary to bring focus
Siddhesh Babanrao Wagh, Ravi Anadure, Vijay Dutta, M S Sandhu, Rahul Trehan   +4 more
openaire   +2 more sources

Effect of Calcium Deficiency on Growth and Leaf Acid Soluble Proteins of Tomato [PDF]

, 2007
The effects of temporary Ca (Ca) calcium deficiency lasting 2, 3, 4 or 5 d were investigated on tomato plants at the 6-leaf stage, grown hydroponically under controlled conditions.
Silvestre, Jérôme, Pinelli, Eric, Baboulène, Laurence, Morard, Philippe   +3 more
core   +1 more source

Nonclassic lipoid congenital adrenal hyperplasia masquerading as familial glucocorticoid deficiency [PDF]

, 2009
Context: Familial glucocorticoid deficiency (FGD) is an autosomal recessive disorder resulting from resistance to the action of ACTH on the adrenal cortex.
Racine, M, Naville, D., Nurnberg, G., Green, J, Metherell, L. A., Nurnberg, P, Krone, NP, Krone, N. P., Arlt, W, Tomlinson, Jeremy, Achermann, JC, Halaby, G, Tomlinson, J. W., Clark, A. J. L., Krone, Nils, Naville, D, Berney, D. M., Begeot, M., Huebner, A., Halaby, G., Green, J., Berney, DM, Clark, AJ, Lin, L, Lin, L., Racine, M., Arlt, Wiebke, Achermann, J. C., Arlt, W., Nurnberg, G, Metherell, LA, Tomlinson, JW, Begeot, M, Huebner, A, Nurnberg, P., Clark, AJL   +35 more
core   +1 more source