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Results: 1 to 20 of 30

1.

Etiologies and early diagnosis of short stature and growth failure in children and adolescents.

Rogol AD, Hayden GF.

J Pediatr. 2014 May;164(5 Suppl):S1-14.e6. doi: 10.1016/j.jpeds.2014.02.027. Review.

PMID:
24731744
2.

Are RASopathies new monogenic predisposing conditions to the development of systemic lupus erythematosus? Case report and systematic review of the literature.

Bader-Meunier B, Cavé H, Jeremiah N, Magerus A, Lanzarotti N, Rieux-Laucat F, Cormier-Daire V.

Semin Arthritis Rheum. 2013 Oct;43(2):217-9. doi: 10.1016/j.semarthrit.2013.04.009. Epub 2013 Jun 17. Review.

PMID:
23786871
3.

Protein tyrosine phosphatase variants in human hereditary disorders and disease susceptibilities.

Hendriks WJ, Pulido R.

Biochim Biophys Acta. 2013 Oct;1832(10):1673-96. doi: 10.1016/j.bbadis.2013.05.022. Epub 2013 May 23. Review.

4.

[Enigmatic lymphatic diseases involving the lung].

Khen-Dunlop N, Amiel J, Delacourt C, Révillon Y.

Rev Pneumol Clin. 2013 Oct;69(5):260-4. doi: 10.1016/j.pneumo.2013.02.001. Epub 2013 Apr 3. Review. French.

PMID:
23561737
5.

Spectrum of insulin-like growth factor deficiency.

Wit JM, Oostdijk W, Losekoot M.

Endocr Dev. 2012;23:30-41. doi: 10.1159/000341739. Epub 2012 Nov 23. Review.

PMID:
23182818
6.

Growth hormone: the expansion of available products and indications.

Franklin SL, Geffner ME.

Pediatr Clin North Am. 2011 Oct;58(5):1141-65, x. doi: 10.1016/j.pcl.2011.07.006. Review.

PMID:
21981953
7.

The diagnostic and clinical significance of café-au-lait macules.

Shah KN.

Pediatr Clin North Am. 2010 Oct;57(5):1131-53. doi: 10.1016/j.pcl.2010.07.002. Review.

PMID:
20888463
8.

Idiopathic bilateral central giant cell reparative granuloma of jaws: a case report and literature review.

Orhan E, Erol S, Deren O, Sevin A, Ekici O, Erdoğan B.

Int J Pediatr Otorhinolaryngol. 2010 May;74(5):547-52. doi: 10.1016/j.ijporl.2010.02.006. Epub 2010 Mar 12. Review.

PMID:
20219254
9.

The molecular genetics of congenital heart disease: a review of recent developments.

Wolf M, Basson CT.

Curr Opin Cardiol. 2010 May;25(3):192-7. doi: 10.1097/HCO.0b013e328337b4ce. Review.

10.

[Children with body length deficiency at birth and at risk of growth deficiency since childhood].

Wiśniewski A.

Pediatr Endocrinol Diabetes Metab. 2009;15(3):210-5. Review. Polish.

PMID:
20384184
11.

[Noonan syndrome: from phenotype to growth hormone therapy].

Malaquias AC, Ferreira LV, Souza SC, Arnhold IJ, Mendonça BB, Jorge AA.

Arq Bras Endocrinol Metabol. 2008 Jul;52(5):800-8. Review. Portuguese.

12.

Leopard syndrome.

Sarkozy A, Digilio MC, Dallapiccola B.

Orphanet J Rare Dis. 2008 May 27;3:13. doi: 10.1186/1750-1172-3-13. Review.

13.

Expanding the genetic spectrum of Noonan syndrome.

Noordam K.

Horm Res. 2007;68 Suppl 5:24-7. doi: 10.1159/000110468. Epub 2007 Dec 10. Review.

PMID:
18174700
14.

Growth hormone therapy in children and adults.

Krysiak R, Gdula-Dymek A, Bednarska-Czerwińska A, Okopień B.

Pharmacol Rep. 2007 Sep-Oct;59(5):500-16. Review.

15.

Central giant cell granuloma of the jaw: a review of the literature with emphasis on therapy options.

de Lange J, van den Akker HP, van den Berg H.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007 Nov;104(5):603-15. Epub 2007 Aug 20. Review.

PMID:
17703964
16.

Genetics of congenital heart diseases in syndromic and non-syndromic patients: new advances and clinical implications.

Piacentini G, Digilio MC, Sarkozy A, Placidi S, Dallapiccola B, Marino B.

J Cardiovasc Med (Hagerstown). 2007 Jan;8(1):7-11. Review.

PMID:
17255809
17.

[The MAP-kinase pathway in genodermatosis: new developments].

Dereure O.

Ann Dermatol Venereol. 2006 Dec;133(12):1031. Review. French. No abstract available.

PMID:
17185943
18.

Inherited predispositions and hyperactive Ras in myeloid leukemogenesis.

Lauchle JO, Braun BS, Loh ML, Shannon K.

Pediatr Blood Cancer. 2006 May 1;46(5):579-85. Review.

PMID:
16261595
19.
20.

Laser-assisted thermal capsulorrhaphy.

Noonan TJ, Tokish JM, Briggs KK, Hawkins RJ.

Arthroscopy. 2003 Oct;19(8):815-9. Review.

PMID:
14551542
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