Hallam L - Search Results

1

A Prospective Study of Sudden Cardiac Death among Children and Young Adults.

Bagnall RD, Weintraub RG, Ingles J, Duflou J, Yeates L, Lam L, Davis AM, Thompson T, Connell V, Wallace J, Naylor C, Crawford J, Love DR, Hallam L, White J, Lawrence C, Lynch M, Morgan N, James P, du Sart D, Puranik R, Langlois N, Vohra J, Winship I, Atherton J, McGaughran J, Skinner JR, Semsarian C. Bagnall RD, et al. Among authors: hallam l. N Engl J Med. 2016 Jun 23;374(25):2441-52. doi: 10.1056/NEJMoa1510687. N Engl J Med. 2016. PMID: 27332903 Free article.

2

Prenatal diagnosis of partial tetrasomy 14: a case study.

George AM, Hallam L, Oei P, McGaughran J. George AM, et al. Among authors: hallam l. Prenat Diagn. 2002 Feb;22(2):127-30. doi: 10.1002/pd.258. Prenat Diagn. 2002. PMID: 11857618

3

Fine needle aspiration biopsy in children.

Orford JE, Gollow I, Brennan B, Hallam L. Orford JE, et al. Among authors: hallam l. Aust N Z J Surg. 1997 Nov;67(11):785-8. doi: 10.1111/j.1445-2197.1997.tb04580.x. Aust N Z J Surg. 1997. PMID: 9396995

4

Clinical and endoscopic predictors of histological oesophagitis in infants.

Chadwick LM, Kurinczuk JJ, Hallam LA, Brennan BA, Forbes D. Chadwick LM, et al. Among authors: hallam la. J Paediatr Child Health. 1997 Oct;33(5):388-93. doi: 10.1111/j.1440-1754.1997.tb01626.x. J Paediatr Child Health. 1997. PMID: 9401880

5

Hereditary gingival fibromatosis with a recessive mode of inheritance. Case reports.

Singer SL, Goldblatt J, Hallam LA, Winters JC. Singer SL, et al. Among authors: hallam la. Aust Dent J. 1993 Dec;38(6):427-32. doi: 10.1111/j.1834-7819.1993.tb04755.x. Aust Dent J. 1993. PMID: 8110075

6

Congenital midline cervical cleft with an underlying bronchogenic like cyst.

Vure S, Pang K, Hallam L, Lui M, Croaker D. Vure S, et al. Among authors: hallam l. Pediatr Surg Int. 2009 Sep;25(9):811-3. doi: 10.1007/s00383-009-2419-6. Epub 2009 Jul 25. Pediatr Surg Int. 2009. PMID: 19633861

7

Enhanced MYCN expression and isochromosome 17q in pineoblastoma cell lines.

Kees UR, Biegel JA, Ford J, Ranford PR, Peroni SE, Hallam LA, Parmiter AH, Willoughby ML, Spagnolo D. Kees UR, et al. Among authors: hallam la. Genes Chromosomes Cancer. 1994 Feb;9(2):129-35. doi: 10.1002/gcc.2870090209. Genes Chromosomes Cancer. 1994. PMID: 7513543

8

A rare case of adenoviral fulminant hepatic necrosis after chemotherapy.

Kaur B, Gottardo NG, Keil AD, Hallam LA, Baker DL. Kaur B, et al. Among authors: hallam la. Pediatr Hematol Oncol. 2002 Jul-Aug;19(5):361-71. doi: 10.1080/08880010290057390. Pediatr Hematol Oncol. 2002. PMID: 12078868

9

A new pineoblastoma cell line, PER-480, with der(10)t(10;17), der(16)t(1;16), and enhanced MYC expression in the absence of gene amplification.

Kees UR, Spagnolo D, Hallam LA, Ford J, Ranford PR, Baker DL, Callen DF, Biegel JA. Kees UR, et al. Among authors: hallam la. Cancer Genet Cytogenet. 1998 Jan 15;100(2):159-64. doi: 10.1016/s0165-4608(97)00030-7. Cancer Genet Cytogenet. 1998. PMID: 9428362

10

Leptomeningeal angiomatosis, absent olfactory tracts, hypoplasia of the cerebellar vermis, cleft lip and palate and congenital heart disease in a stillborn infant.

Hurst JA, Hallam LA, Hockey KA. Hurst JA, et al. Among authors: hallam la. Clin Dysmorphol. 1992 Jul;1(3):168-71. Clin Dysmorphol. 1992. PMID: 1342866 No abstract available.

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