S S Ting
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Explore the profile of S S Ting including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
33
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0
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Recent Articles
1.
Pan K, Ting S, Mohamad A, Lee W, Wong C, Rasit A
Med J Malaysia
. 2004 Jun;
58(5):752-7.
PMID: 15190663
Improvements in the overall treatment of patients with aggressive, large tumours involving the bone have made it possible to preserve and salvage limbs instead of amputating them. Each patient is...
2.
Ting S, Tangye S, Wood J, Ffrench R, Ziegler J
Br J Haematol
. 2001 Apr;
112(4):1004-11.
PMID: 11298599
X-linked severe combined immunodeficiency (XSCID) is a lethal disease resulting in death in infancy. In many instances, haploidentical bone marrow transplantation (BMT) offers reconstitution of T-cell immunity alone, with residual...
3.
Ting S, Leigh D, Lindeman R, Ziegler J
Br J Haematol
. 1999 Aug;
106(1):190-4.
PMID: 10444186
Severe combined immunodeficiency is a heterogenous syndrome of varied genetic origins of which the X-linked type is the commonest (XSCID). The most sensitive method for diagnosis of XSCID in the...
4.
Ting S, Ziegler J, Leigh D, Kemp A, Lindeman R
J Pediatr
. 1998 Oct;
133(4):575-6.
PMID: 9787703
We performed gamma c gene analysis of a boy with severe combined immunodeficiency whose brother died of the same condition. A base pair deletion in exon 6 was found, which...
5.
Ting S, Ziegler J, FISCHER E
J Pediatr
. 1998 Sep;
133(3):450-2.
PMID: 9738733
Blau syndrome is a granulomatous disease of the skin, eyes, and joints, usually without visceral involvement. It is inherited in a autosomal dominant manner. The Blau susceptibility locus has been...
6.
Li S, Ting S, Lindeman R, Ffrench R, Ziegler J
J Paediatr Child Health
. 1998 Jun;
34(3):273-9.
PMID: 9633977
Objective: Carrier identification in X-linked immunodeficiency disorders can be based on the demonstration of non-random X inactivation (NRXI) in affected blood cell lineages when growth is impaired in cells expressing...
7.
Ting S, Ziegler J, Vowels M
Bone Marrow Transplant
. 1998 May;
21(8):841-3.
PMID: 9603413
Children with severe combined immunodeficiency (SCID) have profoundly diminished humoral and cellular immunity resulting in death during infancy unless immune reconstitution occurs by bone marrow transplantation (BMT). Thrombocytopenia post-bone marrow...
8.
Casley W, Allon M, Cousin H, Ting S, Crackower M, Hashimoto L, et al.
Genomics
. 1992 Oct;
14(2):493-4.
PMID: 1330884
Hypokalemic periodic paralysis (HOKPP) is an autosomal dominant neuromuscular disorder characterized by flaccid paralysis accompanied by lowered serum potassium levels. We have tested polymorphic markers linked to the adult skeletal...