Bradley S Miller
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Explore the profile of Bradley S Miller including associated specialties, affiliations and a list of published articles.
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114
Citations
1338
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Recent Articles
1.
Loftus J, Miller B, Parzynski C, Alvir J, Chen Y, Jhingran P, et al.
Ther Adv Endocrinol Metab
. 2025 Feb;
16:20420188241308446.
PMID: 39936080
• Children with growth deficiency (GHD) are often prescribed a growth called to help them grow. • As prescribed, needs to be injected once a day under the skin. Some...
2.
Billington Jr C, Rayannavar A, Tryon R, Kaye T, Gupta A, Lund T, et al.
JAMA Pediatr
. 2025 Feb;
PMID: 39928311
No abstract available.
3.
Rayannavar A, Billington Jr C, Tryon R, Kaye T, Gupta A, Lund T, et al.
Am J Med Genet A
. 2025 Jan;
e63995.
PMID: 39803877
Our objectives are to report on the outcomes of adrenal insufficiency (AI) and cerebral ALD (cALD) in children diagnosed with X-linked adrenoleukodystrophy (ALD) identified by newborn screening (NBS) in Minnesota...
4.
Maniatis A, Cutfield W, Dattani M, Deal C, Collett-Solberg P, Horikawa R, et al.
J Clin Endocrinol Metab
. 2024 Dec;
PMID: 39672599
Context: Several long-acting growth hormone (LAGH) therapies have recently become available, but guidance on their usage in children with growth hormone (GH) deficiency is limited. Methods: International experts in pediatric...
5.
6.
Deal C, Steelman J, Vlachopapadopoulou E, Stawerska R, Silverman L, Phillip M, et al.
Ther Adv Endocrinol Metab
. 2024 Nov;
15:20420188241277404.
PMID: 39526285
• The efficacy of weekly injections was no different from that of daily injections to treat children who don't make enough growth to grow adequately. ○ Efficacy refers to how...
7.
Hoover A, Turcotte L, Phelan R, Barbus C, Rayannavar A, Miller B, et al.
Blood Rev
. 2024 Aug;
68:101225.
PMID: 39107201
Fanconi anemia (FA) is a rare and complex inherited genetic disorder characterized by impaired DNA repair mechanisms leading to genomic instability. Individuals with FA have increased susceptibility to congenital anomalies,...
8.
Lam C, Scaglia F, Berry G, Larson A, Sarafoglou K, Andersson H, et al.
Mol Genet Metab
. 2024 Jul;
142(4):108509.
PMID: 38959600
Objective: Our report describes clinical, genetic, and biochemical features of participants with a molecularly confirmed congenital disorder of glycosylation (CDG) enrolled in the Frontiers in Congenital Disorders of Glycosylation (FCDGC)...
9.
Gupta A, Furcich J, Nascene D, Kemp S, King C, Nolan E, et al.
J Neuroimmunol
. 2024 Jun;
393:578395.
PMID: 38897089
The earliest clinical manifestation of cerebral adrenoleukodystrophy (CALD) is adrenal insufficiency (AI) characterized by elevations in ACTH and loss of cortisol. We showed high (though physiologically achievable) levels of ACTH...
10.
Miller B, Loftus J, Kelkar M, Shrestha S, Parzynski C, Benjumea D, et al.
Endocr Pract
. 2024 May;
30(9):837-846.
PMID: 38821179
Objective: To describe adherence to daily somatropin treatment and impact on height velocity within 1 year of treatment start among patients with pediatric growth hormone deficiency in a real-world US...