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Items: 1 to 20 of 90

1.

A red baby should not be taken too lightly.

Faletra F, Bruno I, Berti I, Pastore S, Pirrone A, Tommasini A.

Acta Paediatr. 2012 Dec;101(12):e573-7. doi: 10.1111/apa.12018. Epub 2012 Sep 23.

PMID:
22946961
2.

Cutaneous graft-versus-host-like histology in childhood. Importance of clonality analysis in differential diagnosis. A case report.

D'hauw A, Seyger MM, Groenen PJ, Weemaes CM, Warris A, Blokx WA.

Br J Dermatol. 2008 May;158(5):1153-6. doi: 10.1111/j.1365-2133.2008.08497.x. Epub 2008 Mar 13. No abstract available.

PMID:
18341659
3.

Dermatologic findings of ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome.

Julapalli MR, Scher RK, Sybert VP, Siegfried EC, Bree AF.

Am J Med Genet A. 2009 Sep;149A(9):1900-6. doi: 10.1002/ajmg.a.32797.

PMID:
19681128
4.

Ocular symptoms and signs in patients with ectodermal dysplasia syndromes.

Kaercher T.

Graefes Arch Clin Exp Ophthalmol. 2004 Jun;242(6):495-500. Epub 2004 Feb 13.

PMID:
14963716
5.

Nuclear factor kappaB essential modulator-deficient child with immunodeficiency yet without anhidrotic ectodermal dysplasia.

Niehues T, Reichenbach J, Neubert J, Gudowius S, Puel A, Horneff G, Lainka E, Dirksen U, Schroten H, Döffinger R, Casanova JL, Wahn V.

J Allergy Clin Immunol. 2004 Dec;114(6):1456-62.

PMID:
15577852
6.

Fatal respiratory syncytial virus infection in severe combined immunodeficiency syndrome.

Milner ME, de la Monte SM, Hutchins GM.

Am J Dis Child. 1985 Nov;139(11):1111-4.

PMID:
3877455
7.

Crohn's disease and idiopathic thrombocytopenic purpura in a patient with ectodermal dysplasia and immunodeficiency.

Motamed F, Zandieh F, Sedighi M.

Iran J Allergy Asthma Immunol. 2006 Sep;5(3):143-5.

8.

Treatment of otorhinolaryngological manifestations of three rare genetic syndromes: Branchio-Oculo-Facial (BOF), Ectrodactyly Ectodermal dysplasia Clefting (EEC) and focal dermal hypoplasia (Goltz syndrome).

Skarzynski H, Podskarbi-Fayette R.

Int J Pediatr Otorhinolaryngol. 2009 Jan;73(1):143-51. doi: 10.1016/j.ijporl.2008.09.021. Epub 2008 Nov 13.

PMID:
19012972
9.

Immunodeficiency problems in children.

Tiller TL Jr, Liddle KJ.

J S C Med Assoc. 2000 May;96(5):225-8. No abstract available.

PMID:
10850027
10.

Cutaneous manifestations of primary immunodeficiency diseases in children.

Moin A, Farhoudi A, Moin M, Pourpak Z, Bazargan N.

Iran J Allergy Asthma Immunol. 2006 Sep;5(3):121-6.

11.

Pathologic changes of skin and hair in ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome.

Dishop MK, Bree AF, Hicks MJ.

Am J Med Genet A. 2009 Sep;149A(9):1935-41. doi: 10.1002/ajmg.a.32826.

PMID:
19697429
12.

[Primary immunodeficiencies. Clinical features and variant forms].

Fontán Casariego G.

Allergol Immunopathol (Madr). 2001 May-Jun;29(3):101-7. Review. Spanish.

PMID:
11434882
13.

Distribution, clinical features and molecular analysis of primary immunodeficiency diseases in Chinese children: a single-center study from 2005 to 2011.

Zhang ZY, An YF, Jiang LP, Liu W, Liu DW, Xie JW, Tang XM, Wang M, Yang XQ, Zhao XD.

Pediatr Infect Dis J. 2013 Oct;32(10):1127-34. doi: 10.1097/INF.0b013e31829aa9e9.

PMID:
23673420
14.

[Severe combined immunodeficiency syndrome. Report of a case--clinical, laboratory and anatomo-pathologic data].

Solé D, Silva MR, Soares FJ, Patrício FS, Naspitz CK.

Rev Paul Med. 1988 Mar-Apr;106(2):75-80. Portuguese. No abstract available.

PMID:
3070704
15.

Human nuclear factor kappa B essential modulator mutation can result in immunodeficiency without ectodermal dysplasia.

Orange JS, Levy O, Brodeur SR, Krzewski K, Roy RM, Niemela JE, Fleisher TA, Bonilla FA, Geha RS.

J Allergy Clin Immunol. 2004 Sep;114(3):650-6.

PMID:
15356572
16.

A rapid screening method to detect autosomal-dominant ectodermal dysplasia with immune deficiency syndrome.

Ohnishi H, Miyata R, Suzuki T, Nose T, Kubota K, Kato Z, Kaneko H, Kondo N.

J Allergy Clin Immunol. 2012 Feb;129(2):578-80. doi: 10.1016/j.jaci.2011.09.042. Epub 2011 Nov 10. No abstract available.

PMID:
22078572
17.

Successful allogeneic hemopoietic stem cell transplantation in a child who had anhidrotic ectodermal dysplasia with immunodeficiency.

Dupuis-Girod S, Cancrini C, Le Deist F, Palma P, Bodemer C, Puel A, Livadiotti S, Picard C, Bossuyt X, Rossi P, Fischer A, Casanova JL.

Pediatrics. 2006 Jul;118(1):e205-11. Epub 2006 Jun 12.

PMID:
16769798
18.

Nasopharyngeal rhabdomyosarcoma in a patient with hypohidrotic ectodermal dysplasia syndrome.

Cankaya H, Kösem M, Kiris M, Uner A, Metin A.

Auris Nasus Larynx. 2002 Jul;29(3):313-6.

PMID:
12167459
19.

Omenn's syndrome: lessons from a red baby.

Katugampola RP, Morgan G, Khetan R, Williams N, Blackford S.

Clin Exp Dermatol. 2008 Jul;33(4):425-8. doi: 10.1111/j.1365-2230.2008.02766.x. Epub 2008 May 21.

PMID:
18498405
20.

X-linked immunodeficiencies.

Ochs HD, Notarangelo LD.

Curr Allergy Asthma Rep. 2004 Sep;4(5):339-48. Review.

PMID:
15283872

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