Gordon B Cutler Jr
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Explore the profile of Gordon B Cutler Jr including associated specialties, affiliations and a list of published articles.
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43
Citations
1161
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Recent Articles
1.
Rodriguez F, Ponce D, Miranda J, Santos J, Cutler Jr G, Pereira A, et al.
Horm Res Paediatr
. 2024 Dec;
1-9.
PMID: 39675347
Introduction: Premature adrenarche in girls is defined biochemically by an increase in adrenal androgen (DHEAS) levels above the age-specific reference range before age 8 years. Recently, increased levels of 11-oxyandrogens...
2.
Merke D, Mallappa A, Parker M, Sukin C, Kulkarni S, Keil M, et al.
J Clin Endocrinol Metab
. 2024 Dec;
PMID: 39672600
Context: Height outcome in patients with classic congenital adrenal hyperplasia (CAH) is suboptimal due to glucocorticoid and androgen excess. Methods: In an open, randomized, controlled trial, children with classic CAH...
3.
Carney P, Cutler Jr G, Schneider K, Zhang F, DiMarchi R
J Clin Endocrinol Metab
. 2024 Nov;
PMID: 39574220
Introduction: Hypoparathyroidism denotes parathyroid hormone (PTH) deficiency and impaired mineral metabolism. MBX 2109, a novel prodrug yielding a biologically active PTH peptide agonist (PTH[1-32], extended by a fatty acylated Lys33),...
4.
Shekhar S, McGlotten R, Cutler Jr G, Crowley M, Pieper C, Nieman L, et al.
J Clin Endocrinol Metab
. 2024 Jul;
110(2):471-479.
PMID: 39013141
Context: Hypogonadism may be caused by Cushing syndrome (CS) and may intensify its adverse consequences. Objective: This work aimed to determine the frequency of male hypogonadism before and after curative...
5.
Auchus R, Hamidi O, Pivonello R, Bancos I, Russo G, Witchel S, et al.
N Engl J Med
. 2024 Jun;
391(6):504-514.
PMID: 38828955
Background: Adrenal insufficiency in patients with classic 21-hydroxylase deficiency congenital adrenal hyperplasia (CAH) is treated with glucocorticoid replacement therapy. Control of adrenal-derived androgen excess usually requires supraphysiologic glucocorticoid dosing, which...
6.
Ponce D, Rodriguez F, Miranda J, Binder A, Santos J, Michels K, et al.
Epigenetics
. 2023 Apr;
18(1):2200366.
PMID: 37053179
Biochemical premature adrenarche is defined by elevated serum DHEAS [≥40 μg/dL] before age 8 y in girls. This condition is receiving more attention due to its association with obesity, hyperinsulinemia,...
7.
Pereira A, Merino P, Santos J, Iniguez G, Cutler Jr G, Corvalan C, et al.
Clin Endocrinol (Oxf)
. 2021 Dec;
96(3):419-427.
PMID: 34904249
Context: An association between premature adrenarche and metabolic syndrome at presentation has been described. Our aim was to assess whether the presence of high dehydroepiandrosterone sulphate (DHEAS [HD]) at the...
8.
Winer K, Ye S, Ferre E, Schmitt M, Zhang B, Cutler Jr G, et al.
Bone
. 2021 May;
149:115977.
PMID: 33932619
Objective: Hypoparathyroidism has heterogeneous genetic and acquired etiologies with a broad spectrum of severity. Herein we describe the clinical outcomes of the largest cohort of hypoparathyroid patients reported to date,...
9.
Child C, Quigley C, Cutler Jr G, Moore W, Wintergerst K, Ross J, et al.
Horm Res Paediatr
. 2019 Jun;
91(4):241-251.
PMID: 31185471
Background/objectives: Growth hormone (GH) treatment of idiopathic short stature (ISS) received US Food and Drug Administration approval in 2003. We assessed height gain and safety in 2,450 children with ISS...
10.
Winer K, Kelly A, Johns A, Zhang B, Dowdy K, Kim L, et al.
J Pediatr
. 2018 Nov;
203:391-399.e1.
PMID: 30470382
Objective: To determine whether multiple daily injections of parathyroid hormone (PTH) 1-34 are safe and effective as long-term therapy for children with hypoparathyroidism. Study Design: Linear growth, bone accrual, renal...