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Showing 1 to 12 of 1264 entries
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An unusual case of rapidly progressive hyperbilirubinemia.

Case reports in pediatrics

Thornton KM, Nyp MF, Music Aplenc L, Jones GL, Carpenter SL, Guest EM, Shapiro SM, Manimtim WM.
PMID: 24288641
Case Rep Pediatr. 2013;2013:284029. doi: 10.1155/2013/284029. Epub 2013 Oct 29.

We present an unusual case of hyperbilirubinemia with rapid early progression leading to bilirubin encephalopathy in a term neonate. Despite early recognition and intervention, the total serum bilirubin reached a maximum level of 39 mg/dL at 32 hours of...

Association between genetic variants of DVWA and osteoarthritis of the knee and hip: a comprehensive meta-analysis.

International journal of clinical and experimental medicine

Zhang R, Yao J, Xu P, Ji B, Voegeli G, Hou W, Li H, Wang Y, Kelsoe JR, Ma J.
PMID: 26309605
Int J Clin Exp Med. 2015 Jun 15;8(6):9430-7. eCollection 2015.

Recently, double von Willebrand factor domain A (DVWA) gene, a previously unknown gene, was revealed to contain several single nucleotide polymorphisms (SNPs) that showed consistent association with knee osteoarthritis (OA) in Japanese and Chinese cohorts. However, subsequent studies failed...

Erratum: Weibel-Palade body size modulates the adhesive activity of its von Willebrand Factor cargo in cultured endothelial cells.

Scientific reports

Ferraro F, da Silva ML, Grimes W, Lee HK, Ketteler R, Kriston-Vizi J, Cutler DF.
PMID: 27666678
Sci Rep. 2016 Sep 26;6:33938. doi: 10.1038/srep33938.

No abstract available.

Diagnosis and Treatment of von Willebrand Disease and Rare Bleeding Disorders.

Journal of clinical medicine

Castaman G, Linari S.
PMID: 28394285
J Clin Med. 2017 Apr 10;6(4). doi: 10.3390/jcm6040045.

Along with haemophilia A and B, von Willebrand disease (VWD) and rare bleeding disorders (RBDs) cover all inherited bleeding disorders of coagulation. Bleeding tendency, which can range from extremely severe to mild, is the common symptom. VWD, due to...

Report on von Willebrand Disease in Malaysia.

Open access Macedonian journal of medical sciences

Periayah MH, Halim AS, Saad AZ, Yaacob NS, Karim FA.
PMID: 27275342
Open Access Maced J Med Sci. 2016 Mar 15;4(1):112-7. doi: 10.3889/oamjms.2016.030. Epub 2016 Feb 29.

BACKGROUND: Von Willebrand disease (vWD) is an inherited hemostatic disorder that affects the hemostasis pathway. The worldwide prevalence of vWD is estimated to be 1% of the general population but only 0.002% in Malaysia.AIM: Our present paper has been...

Gingival enlargement in von Willebrand disease: A case report.

Journal of Indian Society of Periodontology

Gupta P, Jan SM, Behal R, Nazir G.
PMID: 25024557
J Indian Soc Periodontol. 2014 May;18(3):390-4. doi: 10.4103/0972-124X.134587.

von Willebrand disease (vWD) is an inherited bleeding disorder affecting both the sexes with a prevalence of approximately 1% in general population. The cause for bleeding in this disorder can be attributed to the primary deficiency or defect in...

Idiopathic Relapsing Thrombotic Thrombocytopenic Purpura with Persistent ADAMTS13 Inhibitor Activity Treated Sequentially with Plasmapheresis, Rituximab, Cyclophosphamide and Splenectomy.

Case reports in oncology

Musa F, Baidas S.
PMID: 26034479
Case Rep Oncol. 2015 Apr 22;8(1):196-9. doi: 10.1159/000381868. eCollection 2015.

We here describe a patient with an idiopathic thrombotic thrombocytopenic purpura (TTP) secondary to an ADAMTS13 inhibitor that continued to be dependent on plasmapheresis until the patient was treated with rituximab. TTP manifestations subsided with rituximab treatment in spite...

[Correlation of Endothelial Dysfunction With Course of Essential Arterial hypertension in Adolescence].

Kardiologiia

Plotnikova IV, Kovalev IA, Suslova TE, Bezlyak VV.
PMID: 28294839
Kardiologiia. 2015 Mar;55(3):21-26.

AIM: to study laboratory parameters of endothelial dysfunction (ED) and their correlation with risk factors (RF) of cardiovascular diseases at early stages of essential arterial hypertension (AH) in adolescents.MATERIAL AND METHODS: We examined 299 adolescents aged 12 - 18...

Isolation and in vitro culture of vascular endothelial cells from mice.

The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology

Choi S, Kim JA, Kim KC, Suh SH.
PMID: 25605995
Korean J Physiol Pharmacol. 2015 Jan;19(1):35-42. doi: 10.4196/kjpp.2015.19.1.35. Epub 2014 Dec 31.

In cardiovascular disorders, understanding of endothelial cell (EC) function is essential to elucidate the disease mechanism. Although the mouse model has many advantages for in vivo and in vitro research, efficient procedures for the isolation and propagation of primary...

Significant Association between Serum Levels of Von Willebrand Factor (vWF) Antigen with Stages of Cirrhosis.

The Eurasian journal of medicine

Yilmaz VT, Dincer D, Avci AB, Cetinkaya R.
PMID: 25745341
Eurasian J Med. 2015 Feb;47(1):21-5. doi: 10.5152/eajm.2014.0016.

OBJECTIVE: Von Willebrand factor (vWF) is a mediator that increases endotoxemic medium like in cirrhosis. In this study we evaluated the association of serum VWF antigen (Ag) level with the stage of cirrhosis (according to Child-Pugh classification).MATERIALS AND METHODS:...

Identification of peptides released from hot water insoluble fraction of edible bird's nest under simulated gastro-intestinal conditions.

Food research international (Ottawa, Ont.)

Kong HK, Wong KH, Lo SC.
PMID: 29544834
Food Res Int. 2016 Jul;85:19-25. doi: 10.1016/j.foodres.2016.04.002. Epub 2016 Apr 16.

For centuries, edible bird's nest (EBN) has been consumed as a Chinese delicacy. In the past decades, numerous studies reported that water soluble extract of the EBN not only possessed epidermal growth factor, but also associated with a wide...

Acquired Von Willebrand's Syndrome in Systemic Lupus Erythematosus.

Case reports in hematology

Taveras Alam S, Alexis K, Sridharan A, Strakhan M, Elrafei T, Gralla RJ, Reed LJ.
PMID: 25544909
Case Rep Hematol. 2014;2014:208597. doi: 10.1155/2014/208597. Epub 2014 Dec 07.

Acquired von Willebrand syndrome (AVWS) is an uncommon, underdiagnosed, and heterogeneous disease which is increasingly recognized as a cause of bleeding diatheses. Systemic lupus erythematosus (SLE) is an infrequent cause of AVWS. Herein, we report a case of AVWS...

Showing 1 to 12 of 1264 entries