Results 131 to 140 of about 3,553,850 (264)

Personalized multimodal physiological modeling of menstrual cycle dynamics using endocrine, metabolic and wearable signals

Journal of Intelligent Medicine, EarlyView.
Abstract Menstrual cycle tracking remains challenged by the limited physiological scope and inconsistent generalizability of existing wearable‐based approaches, which often rely on individual sensing modalities that incompletely capture the complexity of menstrual physiology.
Ejay Nsugbe, Georgianna Lin
wiley   +1 more source

Combined pituitary hormone deficiency in a patient with an FGFR1 missense variant: case report and literature review. [PDF]

Clin Pediatr Endocrinol, 2022
Sano S, Masunaga Y, Kato F, Fujisawa Y, Saitsu H, Ogata T.   +5 more
europepmc   +1 more source

Long-term effects of growth hormone (GH) on bone mineral status and bone turnover markers in patients with isolated GH deficiency and multiple pituitary hormone deficiency

, 2007
Objective This study was designed to assess the long-term effects of growth hormone (GH) replacement therapy on bone mass and bone turnover markers in children with isolated GH deficiency (IGHD) and multiple pituitary hormone deficiency (MPHD)
Kandemir, Nurgun, E. Nazli Gonc, Gonc, E. Nazli, Nurgun Kandemir   +3 more
core   +1 more source

Early enteral nutrition and neurodevelopment in very low birth weight preterm infants

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objective Very low birth weight (VLBW) preterm infants are at increased risk of neurodevelopmental impairment. Although human milk may promote brain development, the association between type of feeding at discharge and neurodevelopmental outcomes remains uncertain.
Serafina Perrone, Maria Maddalena Brambilla, Virginia Beretta, Sabrina Moretti, Vincenzo Raitano, Chiara Petrolini, Valentina Dell'Orto, Silvia Carloni   +7 more
wiley   +1 more source

A novel heterozygous mutation in POU1F1 is associated with combined pituitary hormone deficiency

, 2017
Mutations in the POU1F1 gene (OMIM#613038) are a rare case of combined pituitary hormone deficiency (CPHD), which is characterized by deficiency of growth hormone, TSH, and prolactin.
Olga Y. Rebrova, Valentina A. Peterkova, Tatiana Y. Shiryaeva, Anna E. Gavrilova, Elena V. Nagaeva, Anatoly N. Tiulpakov   +5 more
core   +1 more source

Paediatric Melanonychia: Diagnosis and Management

JEADV Clinical Practice, EarlyView.
ABSTRACT Longitudinal melanonychia (LM) in children presents unique diagnostic and management challenges that cannot be adequately addressed by applying adult‐based criteria. Unlike in adults, there are no validated clinical, dermoscopic or histopathologic criteria for predicting nail unit melanoma in the paediatric population.
Angela J. Jiang, Erika Koh, Je‐Ho Mun, Dong‐Youn Lee, Matilde Iorizzo, Adam I. Rubin   +5 more
wiley   +1 more source

A Novel Splice-Site Deletion in the POU1F1 Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees. [PDF]

Genes (Basel), 2022
Hassan SS, Abdullah M, Trebusak Podkrajsek K, Musa S, Ibrahim A, Babiker O, Kovac J, Battelino T, Avbelj Stefanija M.   +8 more
europepmc   +1 more source

Developing the Dopamine D3 Receptor (D3R) Antagonist, (R)‐VK4‐116, as a Non‐Opioid Medication for the Treatment of Opioid Use Disorder

Medicinal Research Reviews, EarlyView.
ABSTRACT Opioid use disorder (OUD) remains a major global health challenge, and currently approved treatments (methadone, buprenorphine, and naltrexone) are all opioid receptor‐targeting drugs with limitations in access, adherence, stigma, and use in polysubstance use disorders. Because the dopamine D3 receptor (D3R) is enriched in limbic brain regions
Chia‐Kuei Wu, Yu‐Chih Lin, Junfeng Huang, Bangwei Ding, Pramod Terse, Rahul Nandre, Haksong Jin, Molly Congdon, Kun Shen, Philip Sanderson, Gregory Tawa, Stephanie Mounaud, Marta De Santis, Donald Lo, Elizabeth A. Ottinger, Amy Hauck Newman   +15 more
wiley   +1 more source

Immune checkpoint inhibitor-induced isolated adrenocorticotropic hormone deficiency: a systematic review

Frontiers in Endocrinology
BackgroundImmune checkpoint inhibitor-induced isolated adrenocorticotropic hormone deficiency (IAD) is a rare but potentially fatal disease.MethodsWe comprehensively searched the PubMed database and made a systematic review of immune checkpoint inhibitor-
Fen Wang, Xiaoli Shi, Xuefeng Yu, Yan Yang   +3 more
doaj   +1 more source

Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years. [PDF]

EClinicalMedicine, 2022
Hietamäki J, Kärkinen J, Iivonen AP, Vaaralahti K, Tarkkanen A, Almusa H, Huopio H, Hero M, Miettinen PJ, Raivio T.   +9 more
europepmc   +1 more source