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Increased IGFBP Proteolysis, IGF-I Bioavailability, and Pappalysin Levels in Children With Prader-Willi Syndrome.
Barrios V, Martín-Rivada Á, Martos-Moreno GÁ, Canelles S, Moreno-Macián F, De Mingo-Alemany C, Delvecchio M, Pajno R, Fintini D, Chowen JA, Argente J
J Clin Endocrinol Metab, 109(9):e1776-e1786, 01 Aug 2024
Cited by: 2 articles | PMID: 38141219
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Predictors of adherence to follow-up and treatment success in childhood obesity.
Zamora Auñón A, Guijo Alonso B, De Andrés Esteban EM, Argente J, Martos-Moreno GÁ
An Pediatr (Engl Ed), 100(6):428-437, 03 Jun 2024
Cited by: 0 articles | PMID: 38834436
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Common and uncommon mouse models of growth hormone deficiency.
List EO, Basu R, Berryman DE, Duran-Ortiz S, Martos-Moreno GÁ, Kopchick JJ
Endocr Rev, bnae017, 10 Jun 2024
Cited by: 0 articles | PMID: 38853618
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New insights into the landscape of ALPL gene variants in patients with hypophosphatasia from the Global HPP Registry.
Kishnani PS, Seefried L, Dahir KM, Martos-Moreno GÁ, Linglart A, Petryk A, Mowrey WR, Fang S, Ozono K, Högler W, Rockman-Greenberg C
Am J Med Genet A, 194(11):e63781, 17 Jun 2024
Cited by: 0 articles | PMID: 38884565
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Prepubertal children with obesity have high free IGF-1 levels and accelerated growth despite reduced pappalysin levels.
Martín-Rivada Á, Martos-Moreno GÁ, Guerra-Cantera S, Campillo-Calatayud A, Oxvig C, Frystyk J, Chowen JA, Barrios V, Argente J
J Clin Endocrinol Metab, dgae288, 25 Apr 2024
Cited by: 0 articles | PMID: 38662803
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Effectiveness of asfotase alfa for treatment of adults with hypophosphatasia: results from a global registry.
Kishnani PS, Martos-Moreno GÁ, Linglart A, Petryk A, Messali A, Fang S, Rockman-Greenberg C, Ozono K, Högler W, Seefried L, Dahir KM
Orphanet J Rare Dis, 19(1):109, 08 Mar 2024
Cited by: 4 articles | PMID: 38459585 | PMCID: PMC10921796
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Identifying subgroups of childhood obesity by using multiplatform metabotyping.
Chamoso-Sanchez D, Rabadán Pérez F, Argente J, Barbas C, Martos-Moreno GA, Rupérez FJ
Front Mol Biosci, 10:1301996, 20 Dec 2023
Cited by: 0 articles | PMID: 38174068 | PMCID: PMC10761426
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The Global ALPL gene variant classification project: Dedicated to deciphering variants.
Farman MR, Rehder C, Malli T, Rockman-Greenberg C, Dahir K, Martos-Moreno GÁ, Linglart A, Ozono K, Seefried L, Del Angel G, Webersinke G, Barbazza F, John LK, Delana Mudiyanselage SMA, Högler F, Nading EB, Huggins E, Rush ET, El-Gazzar A, [...] Högler W
Bone, 178:116947, 26 Oct 2023
Cited by: 1 article | PMID: 37898381
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The N221D variant in PCSK1 is highly prevalent in childhood obesity and can influence the metabolic profile.
Guijo B, Argente J, Martos-Moreno GÁ
J Pediatr Endocrinol Metab, 36(12):1140-1145, 26 Oct 2023
Cited by: 0 articles | PMID: 37877373
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Clinical Profiles of Children with Hypophosphatasia prior to Treatment with Enzyme Replacement Therapy: An Observational Analysis from the Global HPP Registry.
Martos-Moreno GÁ, Rockman-Greenberg C, Ozono K, Petryk A, Kishnani PS, Dahir KM, Seefried L, Fang S, Högler W, Linglart A
Horm Res Paediatr, 97(3):233-242, 13 Jul 2023
Cited by: 0 articles | PMID: 37442110 | PMCID: PMC11078328
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Growth and disease burden in children with hypophosphatasia.
Högler W, Linglart A, Petryk A, Kishnani PS, Seefried L, Fang S, Rockman-Greenberg C, Ozono K, Dahir K, Martos-Moreno GÁ
Endocr Connect, 12(5):e220240, 25 Apr 2023
Cited by: 1 article | PMID: 36917043 | PMCID: PMC10160547
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Impact of muscular symptoms and/or pain on disease characteristics, disability, and quality of life in adult patients with hypophosphatasia: A cross-sectional analysis from the Global HPP Registry.
Dahir KM, Kishnani PS, Martos-Moreno GÁ, Linglart A, Petryk A, Rockman-Greenberg C, Martel SE, Ozono K, Högler W, Seefried L
Front Endocrinol (Lausanne), 14:1138599, 27 Mar 2023
Cited by: 4 articles | PMID: 37051203 | PMCID: PMC10083387
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Quality of life improvements following one year of setmelanotide in children and adult patients with Bardet-Biedl syndrome: phase 3 trial results.
Forsythe E, Haws RM, Argente J, Beales P, Martos-Moreno GÁ, Dollfus H, Chirila C, Gnanasakthy A, Buckley BC, Mallya UG, Clément K, Haqq AM
Orphanet J Rare Dis, 18(1):12, 16 Jan 2023
Cited by: 10 articles | PMID: 36647077 | PMCID: PMC9841937
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Efficacy and safety of setmelanotide, a melanocortin-4 receptor agonist, in patients with Bardet-Biedl syndrome and Alström syndrome: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial with an open-label period.
Haqq AM, Chung WK, Dollfus H, Haws RM, Martos-Moreno GÁ, Poitou C, Yanovski JA, Mittleman RS, Yuan G, Forsythe E, Clément K, Argente J
Lancet Diabetes Endocrinol, 10(12):859-868, 07 Nov 2022
Cited by: 33 articles | PMID: 36356613 | PMCID: PMC9847480
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Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.
Grange LJ, Reynolds JJ, Ullah F, Isidor B, Shearer RF, Latypova X, Baxley RM, Oliver AW, Ganesh A, Cooke SL, Jhujh SS, McNee GS, Hollingworth R, Higgs MR, Natsume T, Khan T, Martos-Moreno GÁ, Chupp S, Mathew CG, [...] Stewart GS
Nat Commun, 13(1):6664, 04 Nov 2022
Cited by: 16 articles | PMID: 36333305 | PMCID: PMC9636423
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Carbohydrate metabolism impairment in children and adolescents with cystic fibrosis.
Escudero García J, Martín Rivada Á, Uribe Posada A, Sanz Santiago V, Argente J, Martos-Moreno GÁ
Endocrinol Diabetes Nutr (Engl Ed), 69(8):576-583, 01 Oct 2022
Cited by: 1 article | PMID: 36347795
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Pappalysins and Stanniocalcins and Their Relationship With the Peripheral IGF Axis in Newborns and During Development.
Martín-Rivada Á, Guerra-Cantera S, Campillo-Calatayud A, Andrés-Esteban EM, Sánchez Holgado M, Martos-Moreno GÁ, Pozo J, Güemes M, Soriano-Guillén L, Pellicer A, Oxvig C, Frystyk J, Chowen JA, Barrios V, Argente J
J Clin Endocrinol Metab, 107(10):2912-2924, 01 Sep 2022
Cited by: 7 articles | PMID: 35902207
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Clinical profiles of treated and untreated adults with hypophosphatasia in the Global HPP Registry.
Dahir KM, Seefried L, Kishnani PS, Petryk A, Högler W, Linglart A, Martos-Moreno GÁ, Ozono K, Fang S, Rockman-Greenberg C
Orphanet J Rare Dis, 17(1):277, 19 Jul 2022
Cited by: 10 articles | PMID: 35854311 | PMCID: PMC9295501
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Unveiling Metabolic Phenotype Alterations in Anorexia Nervosa through Metabolomics.
Mayo-Martínez L, Rupérez FJ, Martos-Moreno GÁ, Graell M, Barbas C, Argente J, García A
Nutrients, 13(12):4249, 26 Nov 2021
Cited by: 2 articles | PMID: 34959800 | PMCID: PMC8706417
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Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency.
Akin L, Rizzoti K, Gregory LC, Corredor B, Le Quesne Stabej P, Williams H, Buonocore F, Mouilleron S, Capra V, McGlacken-Byrne SM, Martos-Moreno GÁ, Azmanov DN, Kendirci M, Kurtoglu S, Suntharalingham JP, Galichet C, Gustincich S, Tasic V, Achermann JC, [...] Dattani MT
Genet Med, 24(2):384-397, 30 Nov 2021
Cited by: 1 article | PMID: 34906446 | PMCID: PMC7612377
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Conservative Treatment for Childhood and Adolescent Obesity: Real World Follow-Up Profiling and Clinical Evolution in 1300 Patients.
Martos-Moreno GÁ, Martínez-Villanueva Fernández J, Frías-Herrero A, Martín-Rivada Á, Argente J
Nutrients, 13(11):3847, 28 Oct 2021
Cited by: 2 articles | PMID: 34836102 | PMCID: PMC8624087
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Adult height and long-term outcomes after rhIGF-1 therapy in two patients with PAPP-A2 deficiency.
Martín-Rivada Á, Barrios V, Martínez Díaz-Guerra G, Pozo J, Martos-Moreno GÁ, Argente J
Growth Horm IGF Res, 60-61:101419, 25 Jul 2021
Cited by: 2 articles | PMID: 34358737
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Missplicing due to a synonymous, T96= exonic substitution in the T-box transcription factor TBX19 resulting in isolated ACTH deficiency.
Maudhoo A, Maharaj A, Buonocore F, Martos-Moreno GA, Argente J, Achermann JC, Chan LF, Metherell LA
Endocrinol Diabetes Metab Case Rep, 2021:EDM21-0128, 01 Sep 2021
Cited by: 2 articles | PMID: 34564059 | PMCID: PMC8495723
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Bone Mineral Density, Body Composition, and Metabolic Health of Very Low Birth Weight Infants Fed in Hospital Following Current Macronutrient Recommendations during the First 3 Years of Life.
Mihatsch W, Dorronsoro Martín I, Barrios-Sabador V, Couce ML, Martos-Moreno GÁ, Argente J, Quero J, Saenz de Pipaon M
Nutrients, 13(3):1005, 20 Mar 2021
Cited by: 4 articles | PMID: 33804764 | PMCID: PMC8003951
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The pubertal growth spurt is diminished in children with severe obesity.
Holmgren A, Martos-Moreno GÁ, Niklasson A, Martínez-Villanueva J, Argente J, Albertsson-Wikland K
Pediatr Res, 90(1):184-190, 10 Nov 2020
Cited by: 8 articles | PMID: 33173182
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1-25 of 114 results

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Search life-sciences literature (45,100,050 articles, preprints and more)

Search results

Increased IGFBP Proteolysis, IGF-I Bioavailability, and Pappalysin Levels in Children With Prader-Willi Syndrome.

Predictors of adherence to follow-up and treatment success in childhood obesity.

Common and uncommon mouse models of growth hormone deficiency.

New insights into the landscape of ALPL gene variants in patients with hypophosphatasia from the Global HPP Registry.

Prepubertal children with obesity have high free IGF-1 levels and accelerated growth despite reduced pappalysin levels.

Effectiveness of asfotase alfa for treatment of adults with hypophosphatasia: results from a global registry.

Identifying subgroups of childhood obesity by using multiplatform metabotyping.

The Global ALPL gene variant classification project: Dedicated to deciphering variants.

The N221D variant in PCSK1 is highly prevalent in childhood obesity and can influence the metabolic profile.

Clinical Profiles of Children with Hypophosphatasia prior to Treatment with Enzyme Replacement Therapy: An Observational Analysis from the Global HPP Registry.

Growth and disease burden in children with hypophosphatasia.

Impact of muscular symptoms and/or pain on disease characteristics, disability, and quality of life in adult patients with hypophosphatasia: A cross-sectional analysis from the Global HPP Registry.

Quality of life improvements following one year of setmelanotide in children and adult patients with Bardet-Biedl syndrome: phase 3 trial results.

Efficacy and safety of setmelanotide, a melanocortin-4 receptor agonist, in patients with Bardet-Biedl syndrome and Alström syndrome: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial with an open-label period.

Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.

Carbohydrate metabolism impairment in children and adolescents with cystic fibrosis.

Pappalysins and Stanniocalcins and Their Relationship With the Peripheral IGF Axis in Newborns and During Development.

Clinical profiles of treated and untreated adults with hypophosphatasia in the Global HPP Registry.

Unveiling Metabolic Phenotype Alterations in Anorexia Nervosa through Metabolomics.

Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency.

Conservative Treatment for Childhood and Adolescent Obesity: Real World Follow-Up Profiling and Clinical Evolution in 1300 Patients.

Adult height and long-term outcomes after rhIGF-1 therapy in two patients with PAPP-A2 deficiency.

Missplicing due to a synonymous, T96= exonic substitution in the T-box transcription factor TBX19 resulting in isolated ACTH deficiency.

Bone Mineral Density, Body Composition, and Metabolic Health of Very Low Birth Weight Infants Fed in Hospital Following Current Macronutrient Recommendations during the First 3 Years of Life.

The pubertal growth spurt is diminished in children with severe obesity.

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