Roper HP - Search Results

1

Mild ichthyosis in a 4-year-old boy with multiple sulphatase deficiency.

Loffeld A, Gray RG, Green SH, Roper HP, Moss C. Loffeld A, et al. Among authors: roper hp. Br J Dermatol. 2002 Aug;147(2):353-5. doi: 10.1046/j.1365-2133.2002.04776.x. Br J Dermatol. 2002. PMID: 12174111 Review.

2

Aplasia cutis congenita with chromosome 12q abnormality.

Khan JY, Moss C, Roper HP. Khan JY, et al. Among authors: roper hp. Arch Dis Child Fetal Neonatal Ed. 1995 May;72(3):F205-6. doi: 10.1136/fn.72.3.f205. Arch Dis Child Fetal Neonatal Ed. 1995. PMID: 7796242 Free PMC article.

3

Mitochondrial cytopathy presenting with focal segmental glomerulosclerosis, hypoparathyroidism, sensorineural deafness, and progressive neurological disease.

Hameed R, Raafat F, Ramani P, Gray G, Roper HP, Milford DV. Hameed R, et al. Among authors: roper hp. Postgrad Med J. 2001 Aug;77(910):523-6. doi: 10.1136/pmj.77.910.523. Postgrad Med J. 2001. PMID: 11470934 Free PMC article.

4

Lamotrigine poisoning presenting as seizures: a case of deliberate poisoning.

Willis T, Roper H, Rabb L. Willis T, et al. Child Abuse Negl. 2007 Jan;31(1):85-8. doi: 10.1016/j.chiabu.2006.04.009. Epub 2007 Jan 4. Child Abuse Negl. 2007. PMID: 17207854

5

Neuromuscular diseases in children.

Roper HP. Roper HP. Br J Hosp Med. 1993 Apr 21-May 4;49(8):537, 540-5. Br J Hosp Med. 1993. PMID: 8508238 Review.

6

Implementation of "the consensus statement for the standard of care in spinal muscular atrophy" when applied to infants with severe type 1 SMA in the UK.

Roper H, Quinlivan R; Workshop Participants. Roper H, et al. Arch Dis Child. 2010 Oct;95(10):845-9. doi: 10.1136/adc.2009.166512. Epub 2009 Oct 8. Arch Dis Child. 2010. PMID: 19819869 Review.

7

Variable presentation of primary hyperoxaluria type 1 in 2 patients homozygous for a novel combined deletion and insertion mutation in exon 8 of the AGXT gene.

von Schnakenburg C, Hulton SA, Milford DV, Roper HP, Rumsby G. von Schnakenburg C, et al. Among authors: roper hp. Nephron. 1998;78(4):485-8. doi: 10.1159/000044979. Nephron. 1998. PMID: 9578076

8

Pulmonary hypertension resulting from upper airways obstruction in Down's syndrome.

Ayeni TI, Roper HP. Ayeni TI, et al. Among authors: roper hp. J R Soc Med. 1998 Jun;91(6):321-2. doi: 10.1177/014107689809100612. J R Soc Med. 1998. PMID: 9771520 Free PMC article. No abstract available.

9

Developing standardized corticosteroid treatment for Duchenne muscular dystrophy.

Guglieri M, Bushby K, McDermott MP, Hart KA, Tawil R, Martens WB, Herr BE, McColl E, Wilkinson J, Kirschner J, King WM, Eagle M, Brown MW, Willis T, Hirtz D, Shieh PB, Straub V, Childs AM, Ciafaloni E, Butterfield RJ, Horrocks I, Spinty S, Flanigan KM, Kuntz NL, Baranello G, Roper H, Morrison L, Mah JK, Manzur AY, McDonald CM, Schara U, von der Hagen M, Barohn RJ, Campbell C, Darras BT, Finkel RS, Vita G, Hughes I, Mongini T, Pegoraro E, Wicklund M, Wilichowski E, Bryan Burnette W, Howard JF, McMillan HJ, Thangarajh M, Griggs RC. Guglieri M, et al. Contemp Clin Trials. 2017 Jul;58:34-39. doi: 10.1016/j.cct.2017.04.008. Epub 2017 Apr 24. Contemp Clin Trials. 2017. PMID: 28450193 Free PMC article. Clinical Trial.

10

Randomised placebo-controlled trial of combination ACE inhibitor and beta-blocker therapy to prevent cardiomyopathy in children with Duchenne muscular dystrophy? (DMD Heart Protection Study): a protocol study.

Bourke JP, Watson G, Muntoni F, Spinty S, Roper H, Guglieri M, Speed C, McColl E, Chikermane A, Jayawant S, Adwani S, Willis T, Wilkinson J, Bryant A, Chadwick T, Wood R, Bushby K; DMD Heart Protection study group. Bourke JP, et al. BMJ Open. 2018 Dec 19;8(12):e022572. doi: 10.1136/bmjopen-2018-022572. BMJ Open. 2018. PMID: 30573480 Free PMC article.

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