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Results: 1 to 20 of 391

1.

Sporadic paraganglioma caused by de novo SDHB mutations in a 6-year-old girl.

Imamura H, Muroya K, Tanaka E, Konomoto T, Moritake H, Sato T, Kimura N, Takekoshi K, Nunoi H.

Eur J Pediatr. 2015 Aug 19. [Epub ahead of print]

PMID:
26283294
2.

Morbidity and medication in a large population of individuals with Down syndrome compared to the general population.

Alexander M, Petri H, Ding Y, Wandel C, Khwaja O, Foskett N.

Dev Med Child Neurol. 2015 Aug 18. doi: 10.1111/dmcn.12868. [Epub ahead of print]

PMID:
26282180
3.

Myocardial Performance Index in Childhood Onset Essential Hypertension and White Coat Hypertension.

Gupta-Malhotra M, Hamzeh RK, Poffenbarger T, McNiece-Redwine K, Hashmi SS.

Am J Hypertens. 2015 Aug 12. pii: hpv123. [Epub ahead of print]

PMID:
26271107
4.

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism.

Scholl UI, Stölting G, Nelson-Williams C, Vichot AA, Choi M, Loring E, Prasad ML, Goh G, Carling T, Juhlin CC, Quack I, Rump LC, Thiel A, Lande M, Frazier BG, Rasoulpour M, Bowlin DL, Sethna CB, Trachtman H, Fahlke C, Lifton RP.

Elife. 2015 Apr 24;4:e06315. doi: 10.7554/eLife.06315.

5.

Endocrine Hypertension in Childhood.

Nimkarn S.

In: De Groot LJ, Beck-Peccoz P, Chrousos G, Dungan K, Grossman A, Hershman JM, Koch C, McLachlan R, New M, Rebar R, Singer F, Vinik A, Weickert MO, editors. Endotext [Internet]. South Dartmouth (MA): MDText.com, Inc.; 2000-.
2013 Jun 19.

6.

Special Considerations Relative to Pediatric Obesity.

Rosenbaum M.

In: De Groot LJ, Beck-Peccoz P, Chrousos G, Dungan K, Grossman A, Hershman JM, Koch C, McLachlan R, New M, Rebar R, Singer F, Vinik A, Weickert MO, editors. Endotext [Internet]. South Dartmouth (MA): MDText.com, Inc.; 2000-.
2013 Apr 8.

7.

Obesity and the metabolic syndrome in pediatric psoriasis.

Gutmark-Little I, Shah KN.

Clin Dermatol. 2015 May-Jun;33(3):305-15. doi: 10.1016/j.clindermatol.2014.12.006. Epub 2014 Dec 10.

PMID:
25889131
8.

Takayasu arteritis in childhood: retrospective experience from a tertiary referral centre in the United Kingdom.

Eleftheriou D, Varnier G, Dolezalova P, McMahon AM, Al-Obaidi M, Brogan PA.

Arthritis Res Ther. 2015 Feb 25;17:36. doi: 10.1186/s13075-015-0545-1.

9.

[Childhood-onset systemic polyarteritis nodosa and systemic lupus erythematosus: an overlap syndrome?]

Marques VL, Guariento A, Simões MS, Blay G, Lotito AP, Silva CA.

Rev Bras Reumatol. 2015 Mar 4. pii: S0482-5004(15)00029-7. doi: 10.1016/j.rbr.2015.01.004. [Epub ahead of print] Portuguese.

10.

Early onset hearing loss in autosomal recessive hypophosphatemic rickets caused by loss of function mutation in ENPP1.

Steichen-Gersdorf E, Lorenz-Depiereux B, Strom TM, Shaw NJ.

J Pediatr Endocrinol Metab. 2015 Jul 1;28(7-8):967-70. doi: 10.1515/jpem-2014-0531.

PMID:
25741938
11.

Clinical manifestation of Fuchs uveitis syndrome in childhood.

Tappeiner C, Dreesbach J, Roesel M, Heinz C, Heiligenhaus A.

Graefes Arch Clin Exp Ophthalmol. 2015 Jul;253(7):1169-74. doi: 10.1007/s00417-015-2960-z. Epub 2015 Feb 19.

PMID:
25694152
12.

Microvascular Complications in Childhood-Onset Type 1 Diabetes and Celiac Disease: A Multicenter Longitudinal Analysis of 56,514 Patients From the German-Austrian DPV Database.

Rohrer TR, Wolf J, Liptay S, Zimmer KP, Fröhlich-Reiterer E, Scheuing N, Marg W, Stern M, Kapellen TM, Hauffa BP, Wölfle J, Holl RW; DPV Initiative and the German BMBF Competence Network Diabetes Mellitus.

Diabetes Care. 2015 May;38(5):801-7. doi: 10.2337/dc14-0683. Epub 2015 Feb 17.

PMID:
25690004
13.

A case of functional growth hormone deficiency and early growth retardation in a child with IFT172 mutations.

Lucas-Herald AK, Kinning E, Iida A, Wang Z, Miyake N, Ikegawa S, McNeilly J, Ahmed SF.

J Clin Endocrinol Metab. 2015 Apr;100(4):1221-4. doi: 10.1210/jc.2014-3852. Epub 2015 Feb 9.

PMID:
25664603
14.

Childhood sarcoidosis: Louisiana experience.

Gedalia A, Khan TA, Shetty AK, Dimitriades VR, Espinoza LR.

Clin Rheumatol. 2015 Jan 24. [Epub ahead of print]

PMID:
25616361
15.

[Obesity and cardiovascular risk in children].

Shashaj B, Graziani MP, Tozzi AE, Manco M.

Recenti Prog Med. 2014 Dec;105(12):454-6. doi: 10.1701/1706.18614. Italian.

PMID:
25533232
16.

Subclinical right ventricle systolic dysfunction in childhood-onset systemic lupus erythematosus: insights from two-dimensional speckle-tracking echocardiography.

Leal GN, Silva KF, França CM, Lianza AC, Andrade JL, Campos LM, Bonfá E, Silva CA.

Lupus. 2015 May;24(6):613-20. doi: 10.1177/0961203314563135. Epub 2014 Dec 8.

PMID:
25492941
17.

Complications and comorbidities of T2DM in adolescents: findings from the TODAY clinical trial.

Tryggestad JB, Willi SM.

J Diabetes Complications. 2015 Mar;29(2):307-12. doi: 10.1016/j.jdiacomp.2014.10.009. Epub 2014 Oct 29. Review.

PMID:
25468310
18.

Vascular comorbidities in the onset and progression of multiple sclerosis.

Tettey P, Simpson S Jr, Taylor BV, van der Mei IA.

J Neurol Sci. 2014 Dec 15;347(1-2):23-33. doi: 10.1016/j.jns.2014.10.020. Epub 2014 Oct 16. Review.

PMID:
25454639
19.

Penetrance and clinical features of pheochromocytoma in a six-generation family carrying a germline TMEM127 mutation.

Toledo SP, Lourenço DM Jr, Sekiya T, Lucon AM, Baena ME, Castro CC, Bortolotto LA, Zerbini MC, Siqueira SA, Toledo RA, Dahia PL.

J Clin Endocrinol Metab. 2015 Feb;100(2):E308-18. doi: 10.1210/jc.2014-2473. Epub 2014 Nov 12.

PMID:
25389632
20.

TMEM70 deficiency: long-term outcome of 48 patients.

Magner M, Dvorakova V, Tesarova M, Mazurova S, Hansikova H, Zahorec M, Brennerova K, Bzduch V, Spiegel R, Horovitz Y, Mandel H, Eminoğlu FT, Mayr JA, Koch J, Martinelli D, Bertini E, Konstantopoulou V, Smet J, Rahman S, Broomfield A, Stojanović V, Dionisi-Vici C, van Coster R, Morava E, Sperl W, Zeman J, Honzik T.

J Inherit Metab Dis. 2015 May;38(3):417-26. doi: 10.1007/s10545-014-9774-8. Epub 2014 Oct 18. Erratum in: J Inherit Metab Dis. 2015 May;38(3):583-4. Morava-Kozicz, Eva [corrected to Morava, Eva].

PMID:
25326274
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