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Items: 1 to 20 of 273

1.

The fluid membrane determines mechanics of erythrocyte extracellular vesicles and is softened in hereditary spherocytosis.

Vorselen D, van Dommelen SM, Sorkin R, Piontek MC, Schiller J, Döpp ST, Kooijmans SAA, van Oirschot BA, Versluijs BA, Bierings MB, van Wijk R, Schiffelers RM, Wuite GJL, Roos WH.

Nat Commun. 2018 Nov 23;9(1):4960. doi: 10.1038/s41467-018-07445-x.

2.

Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.

Bianchi P, Fermo E, Glader B, Kanno H, Agarwal A, Barcellini W, Eber S, Hoyer JD, Kuter DJ, Maia TM, Mañu-Pereira MDM, Kalfa TA, Pissard S, Segovia JC, van Beers E, Gallagher PG, Rees DC, van Wijk R; with the endorsement of EuroBloodNet, the European Reference Network in Rare Hematological Diseases.

Am J Hematol. 2018 Oct 25. doi: 10.1002/ajh.25325. [Epub ahead of print]

PMID:
30358897
3.

Organ involvement occurs in all forms of hereditary haemolytic anaemia.

van Straaten S, Verhoeven J, Hagens S, Schutgens R, van Solinge W, van Wijk R, van Beers EJ.

Br J Haematol. 2018 Sep 5. doi: 10.1111/bjh.15575. [Epub ahead of print] No abstract available.

PMID:
30183081
4.

Application of delayed luminescence method on measuring of the processing of Chinese herbal materials.

Sun M, Chang WT, Van Wijk E, He M, Van Wijk R, Wang M.

Chin Med. 2018 Aug 25;13:43. doi: 10.1186/s13020-018-0202-0. eCollection 2018.

5.

Loss-of-function zinc finger mutation in the EGLN1 gene associated with erythrocytosis.

Sinnema M, Song D, Guan W, Janssen JWH, van Wijk R, Navalsky BE, Peng K, Donker AE, Stegmann APA, Lee FS.

Blood. 2018 Sep 27;132(13):1455-1458. doi: 10.1182/blood-2018-06-854711. Epub 2018 Aug 15. No abstract available.

PMID:
30111608
6.

Knock-Down of Arabidopsis PLC5 Reduces Primary Root Growth and Secondary Root Formation While Overexpression Improves Drought Tolerance and Causes Stunted Root Hair Growth.

Zhang Q, van Wijk R, Zarza X, Shahbaz M, van Hooren M, Guardia A, Scuffi D, García-Mata C, Van den Ende W, Hoffmann-Benning S, Haring MA, Laxalt AM, Munnik T.

Plant Cell Physiol. 2018 Oct 1;59(10):2004-2019. doi: 10.1093/pcp/pcy120.

PMID:
30107538
7.

Iron overload in patients with rare hereditary hemolytic anemia: Evidence-based suggestion on whom and how to screen.

van Straaten S, Biemond BJ, Kerkhoffs JL, Gitz-Francois J, van Wijk R, van Beers EJ.

Am J Hematol. 2018 Nov;93(11):E374-E376. doi: 10.1002/ajh.25251. Epub 2018 Sep 21. No abstract available.

8.

Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosis.

Orvain C, Da Costa L, Van Wijk R, Pissard S, Picard V, Mansour-Hendili L, Cunat S, Giansily-Blaizot M, Cartron G, Schved JF, Aguilar-Martinez P.

Eur J Haematol. 2018 Oct;101(4):566-569. doi: 10.1111/ejh.13135. Epub 2018 Aug 31.

PMID:
29969830
9.

Squeezing for Life - Properties of Red Blood Cell Deformability.

Huisjes R, Bogdanova A, van Solinge WW, Schiffelers RM, Kaestner L, van Wijk R.

Front Physiol. 2018 Jun 1;9:656. doi: 10.3389/fphys.2018.00656. eCollection 2018. Review.

10.

Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease.

Lenglet M, Robriquet F, Schwarz K, Camps C, Couturier A, Hoogewijs D, Buffet A, Knight SJL, Gad S, Couvé S, Chesnel F, Pacault M, Lindenbaum P, Job S, Dumont S, Besnard T, Cornec M, Dreau H, Pentony M, Kvikstad E, Deveaux S, Burnichon N, Ferlicot S, Vilaine M, Mazzella JM, Airaud F, Garrec C, Heidet L, Irtan S, Mantadakis E, Bouchireb K, Debatin KM, Redon R, Bezieau S, Bressac-de Paillerets B, Teh BT, Girodon F, Randi ML, Putti MC, Bours V, Van Wijk R, Göthert JR, Kattamis A, Janin N, Bento C, Taylor JC, Arlot-Bonnemains Y, Richard S, Gimenez-Roqueplo AP, Cario H, Gardie B.

Blood. 2018 Aug 2;132(5):469-483. doi: 10.1182/blood-2018-03-838235. Epub 2018 Jun 11.

PMID:
29891534
11.

Quantitative measurement of red cell surface protein expression reveals new biomarkers for hereditary spherocytosis.

Huisjes R, Satchwell TJ, Verhagen LP, Schiffelers RM, van Solinge WW, Toye AM, van Wijk R.

Int J Lab Hematol. 2018 Aug;40(4):e74-e77. doi: 10.1111/ijlh.12841. Epub 2018 May 10. No abstract available.

PMID:
29746727
12.

Oxidative stress in sickle cell disease; more than a DAMP squib.

van Beers EJ, van Wijk R.

Clin Hemorheol Microcirc. 2018;68(2-3):239-250. doi: 10.3233/CH-189010.

PMID:
29614635
13.

Arabidopsis Phospholipase C3 is Involved in Lateral Root Initiation and ABA Responses in Seed Germination and Stomatal Closure.

Zhang Q, van Wijk R, Shahbaz M, Roels W, Schooten BV, Vermeer JEM, Zarza X, Guardia A, Scuffi D, García-Mata C, Laha D, Williams P, Willems LAJ, Ligterink W, Hoffmann-Benning S, Gillaspy G, Schaaf G, Haring MA, Laxalt AM, Munnik T.

Plant Cell Physiol. 2018 Mar 1;59(3):469-486. doi: 10.1093/pcp/pcx194.

PMID:
29309666
14.

Worldwide study of hematopoietic allogeneic stem cell transplantation in pyruvate kinase deficiency.

van Straaten S, Bierings M, Bianchi P, Akiyoshi K, Kanno H, Serra IB, Chen J, Huang X, van Beers E, Ekwattanakit S, Güngör T, Kors WA, Smiers F, Raymakers R, Yanez L, Sevilla J, van Solinge W, Segovia JC, van Wijk R.

Haematologica. 2018 Feb;103(2):e82-e86. doi: 10.3324/haematol.2017.177857. Epub 2017 Dec 14. No abstract available.

15.

Digital microscopy as a screening tool for the diagnosis of hereditary hemolytic anemia.

Huisjes R, van Solinge WW, Levin MD, van Wijk R, Riedl JA.

Int J Lab Hematol. 2018 Apr;40(2):159-168. doi: 10.1111/ijlh.12758. Epub 2017 Nov 1.

PMID:
29090523
16.

Is Increased Intracellular Calcium in Red Blood Cells a Common Component in the Molecular Mechanism Causing Anemia?

Hertz L, Huisjes R, Llaudet-Planas E, Petkova-Kirova P, Makhro A, Danielczok JG, Egee S, Del Mar Mañú-Pereira M, van Wijk R, Vives Corrons JL, Bogdanova A, Kaestner L.

Front Physiol. 2017 Sep 6;8:673. doi: 10.3389/fphys.2017.00673. eCollection 2017.

17.

A histomorphometric study on the effects of antiretroviral therapy (ART) combined with a high-calorie diet (HCD) on aortic perivascular adipose tissue (PVAT).

Nel S, Strijdom H, Genis A, Everson F, Van Wijk R, Kotzé SH.

Acta Histochem. 2017 Jun;119(5):555-562. doi: 10.1016/j.acthis.2017.05.009. Epub 2017 Jun 9.

PMID:
28606728
18.

Profound spherocytosis in adulthood: Acquired, hereditary or both?

Langeveld TJC, van Rossum AP, van der Zwaag B, van Wijk R, Vlasveld LT.

Int J Lab Hematol. 2017 Oct;39(5):e117-e120. doi: 10.1111/ijlh.12685. Epub 2017 May 10. No abstract available.

PMID:
28488802
19.

Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families.

Fermo E, Vercellati C, Marcello AP, Zaninoni A, van Wijk R, Mirra N, Curcio C, Cortelezzi A, Zanella A, Barcellini W, Bianchi P.

Case Rep Hematol. 2017;2017:2769570. doi: 10.1155/2017/2769570. Epub 2017 Mar 6.

20.

Spontaneous ultra-weak photon emission in correlation to inflammatory metabolism and oxidative stress in a mouse model of collagen-induced arthritis.

He M, van Wijk E, van Wietmarschen H, Wang M, Sun M, Koval S, van Wijk R, Hankemeier T, van der Greef J.

J Photochem Photobiol B. 2017 Mar;168:98-106. doi: 10.1016/j.jphotobiol.2016.12.036. Epub 2017 Feb 3.

PMID:
28199905

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