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Items: 1 to 20 of 85

1.

Multisystem disorder of Punjabi children exhibiting spontaneous dermal and submucosal granulation tissue formation: LOGIC syndrome.

Ainsworth JR, Shabbir G, Spencer AF, Cockburn F.

Clin Dysmorphol. 1992 Jan;1(1):3-15.

PMID:
1342856
2.

Laryngeal and ocular granulation tissue formation in two Punjabi children: LOGIC syndrome.

Ainsworth JR, Spencer AF, Dudgeon J, Geddes NK, Lee WR.

Eye (Lond). 1991;5 ( Pt 6):717-22.

PMID:
1800173
3.

Laryngo-onycho-cutaneous syndrome associated with familial benign hypercalcemia.

Handley J, Walsh M, Carson D, Burrows D, Nevin N.

J Am Acad Dermatol. 1993 Nov;29(5 Pt 2):906-9.

PMID:
8408839
4.

Laryngo-onycho-cutaneous syndrome.

Kadyan A, Aralikatti A, Shah S, Jewell R, Paul L, Darling J, Wood M, Gooi J, Morrell AJ, Newton Bishop JA, Marr JE.

Ophthalmology. 2010 May;117(5):1056-1056.e2. doi: 10.1016/j.ophtha.2009.11.019. No abstract available.

PMID:
20438980
5.

Ocular surface reconstruction in LOGIC syndrome by amniotic membrane transplantation.

Moore JE, Dua HS, Page AB, Irvine AD, Archer DB.

Cornea. 2001 Oct;20(7):753-6.

PMID:
11588430
6.

Laryngo-onycho-cutaneous syndrome: an inherited epithelial defect.

Phillips RJ, Atherton DJ, Gibbs ML, Strobel S, Lake BD.

Arch Dis Child. 1994 Apr;70(4):319-26.

7.

Follow up of patients with ocular scarring secondary to LOC syndrome treated by amniotic membrane transplantation.

Moore JE, Shah S, Kumar V, Ainsworth JR, Page AB, McLean WH.

Br J Ophthalmol. 2005 Aug;89(8):939-41.

8.

An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome.

McLean WH, Irvine AD, Hamill KJ, Whittock NV, Coleman-Campbell CM, Mellerio JE, Ashton GS, Dopping-Hepenstal PJ, Eady RA, Jamil T, Phillips R, Shabbir SG, Haroon TS, Khurshid K, Moore JE, Page B, Darling J, Atherton DJ, Van Steensel MA, Munro CS, Smith FJ, McGrath JA.

Hum Mol Genet. 2003 Sep 15;12(18):2395-409. Epub 2003 Jul 15. Erratum in: Hum Mol Genet. 2004 Feb 1;13(3):365. Phillips Rodney J [corrected to Phillips Roderic J].

9.

Micro syndrome in Muslim Pakistan children.

Ainsworth JR, Morton JE, Good P, Woods CG, George ND, Shield JP, Bradbury J, Henderson MJ, Chhina J.

Ophthalmology. 2001 Mar;108(3):491-7.

PMID:
11237903
10.

A child with laryngo-onychocutaneous syndrome partially responsive to treatment with thalidomide.

Strauss RM, Bäte J, Nischal KK, Clayton T, Gooi J, Darling JC, Newton-Bishop JA.

Br J Dermatol. 2006 Dec;155(6):1283-6.

PMID:
17107403
11.

Consanguinity and early mortality in the Muslim populations of India and Pakistan.

Hussain R, Bittles AH, Sullivan S.

Am J Hum Biol. 2001 Nov-Dec;13(6):777-87.

PMID:
11748817
12.

Cancer and congenital abnormalities in Asian children: a population-based study from the West Midlands.

Powell JE, Kelly AM, Parkes SE, Cole TR, Mann JR.

Br J Cancer. 1995 Dec;72(6):1563-9.

13.

Dermatological manifestations of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome.

Collins SM, Dominguez M, Ilmarinen T, Costigan C, Irvine AD.

Br J Dermatol. 2006 Jun;154(6):1088-93.

PMID:
16704638
14.

Histopathologic fundamentals of acquired laryngeal stenosis.

Liu H, Chen JC, Holinger LD, Gonzalez-Crussi F.

Pediatr Pathol Lab Med. 1995 Sep-Oct;15(5):655-77. Review.

PMID:
8597854
15.

Werner's syndrome.

Duvic M, Lemak NA.

Dermatol Clin. 1995 Jan;13(1):163-8. Review.

PMID:
7712642
16.

Airway pathologic abnormalities in symptomatic children with congenital cardiac and vascular disease.

Guillemaud JP, El-Hakim H, Richards S, Chauhan N.

Arch Otolaryngol Head Neck Surg. 2007 Jul;133(7):672-6.

PMID:
17638780
17.

[Familial amyloidosis of the Andrade disease type in a Greek family].

Laskaratos J, Fronimopoulos J.

Klin Monbl Augenheilkd. 1987 May;190(5):439-41. German.

PMID:
3613447
18.

Submucosal arytenoidectomy: new surgical technique and review of the literature.

Danino J, Goldenberg D, Joachims HZ.

J Otolaryngol. 2000 Feb;29(1):13-6. Review.

PMID:
10709166
19.

Spinal tuberculosis: with reference to the children of northern India.

Kumar R.

Childs Nerv Syst. 2005 Jan;21(1):19-26. Epub 2004 Sep 30.

PMID:
15459785
20.

MIDAS syndrome respectively MLS syndrome: a separate entity rather than a particular lyonization pattern of the gene causing Goltz syndrome.

Mücke J, Happle R, Theile H.

Am J Med Genet. 1995 May 22;57(1):117-8. No abstract available.

PMID:
7645589
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