Bellingham A - Search Results

1

Rapid Prototyping of Slot Die Devices for Roll to Roll Production of EL Fibers.

Bellingham A, Bromhead N, Fontecchio A. Bellingham A, et al. Materials (Basel). 2017 May 29;10(6):594. doi: 10.3390/ma10060594. Materials (Basel). 2017. PMID: 28772954 Free PMC article.

2

Passivated aluminum nanohole arrays for label-free biosensing applications.

Canalejas-Tejero V, Herranz S, Bellingham A, Moreno-Bondi MC, Barrios CA. Canalejas-Tejero V, et al. Among authors: bellingham a. ACS Appl Mater Interfaces. 2014 Jan 22;6(2):1005-10. doi: 10.1021/am404509f. Epub 2013 Dec 31. ACS Appl Mater Interfaces. 2014. PMID: 24354280

3

Reversal of metabolic block in glycolysis by enzyme replacement in triosephosphate isomerase-deficient cells.

Ationu A, Humphries A, Lalloz MR, Arya R, Wild B, Warrilow J, Morgan J, Bellingham AJ, Layton DM. Ationu A, et al. Among authors: bellingham aj. Blood. 1999 Nov 1;94(9):3193-8. Blood. 1999. PMID: 10556207 Free article.

4

Porphyrins in urine, plasma, erythrocytes, bile and faeces in a case of congenital erythropoietic porphyria (Gunther's disease) treated with blood transfusion and iron chelation: lack of benefit from oral charcoal.

Gorchein A, Guo R, Lim CK, Raimundo A, Pullon HW, Bellingham AJ. Gorchein A, et al. Among authors: bellingham aj. Biomed Chromatogr. 1998 Nov-Dec;12(6):350-6. doi: 10.1002/(SICI)1099-0801(199811/12)12:6<350::AID-BMC761>3.0.CO;2-B. Biomed Chromatogr. 1998. PMID: 9861496

5

Metabolic correction of triose phosphate isomerase deficiency in vitro by complementation.

Ationu A, Humphries A, Bellingham A, Layton M. Ationu A, et al. Among authors: bellingham a. Biochem Biophys Res Commun. 1997 Mar 17;232(2):528-31. doi: 10.1006/bbrc.1997.6316. Biochem Biophys Res Commun. 1997. PMID: 9125215

6

Evidence for founder effect of the Glu104Asp substitution and identification of new mutations in triosephosphate isomerase deficiency.

Arya R, Lalloz MR, Bellingham AJ, Layton DM. Arya R, et al. Among authors: bellingham aj. Hum Mutat. 1997;10(4):290-4. doi: 10.1002/(SICI)1098-1004(1997)10:4<290::AID-HUMU4>3.0.CO;2-L. Hum Mutat. 1997. PMID: 9338582

7

Hydroxyurea, sickle cell disease and renal transplantation.

Allen A, Scoble J, Snowden S, Hambley H, Bellingham A. Allen A, et al. Among authors: bellingham a. Nephron. 1997;75(1):106-7. doi: 10.1159/000189511. Nephron. 1997. PMID: 9031282 Free article. No abstract available.

8

Two novel mutations in the reduced nicotinamide adenine dinucleotide (NADH)-cytochrome b5 reductase gene of a patient with generalized type, hereditary methemoglobinemia.

Manabe J, Arya R, Sumimoto H, Yubisui T, Bellingham AJ, Layton DM, Fukumaki Y. Manabe J, et al. Among authors: bellingham aj. Blood. 1996 Oct 15;88(8):3208-15. Blood. 1996. PMID: 8874222 Free article.

9

Tucaresol increases oxygen affinity and reduces haemolysis in subjects with sickle cell anaemia.

Arya R, Rolan PE, Wootton R, Posner J, Bellingham AJ. Arya R, et al. Among authors: bellingham aj. Br J Haematol. 1996 Jun;93(4):817-21. doi: 10.1046/j.1365-2141.1996.d01-1744.x. Br J Haematol. 1996. PMID: 8703810 Clinical Trial.

10

Prenatal diagnosis of triosephosphate isomerase deficiency.

Arya R, Lalloz MR, Nicolaides KH, Bellingham AJ, Layton DM. Arya R, et al. Among authors: bellingham aj. Blood. 1996 Jun 1;87(11):4507-9. Blood. 1996. PMID: 8639817 Free article.

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