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

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1-14 of 14 results

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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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Use of [¹⁸F]fluorocholine PET/CT in the detection of primary hyperparathyroidism in paediatrics: a case report.
Martínez Sánchez H, Moreno Macián F, León Cariñena S, de Mingo Alemany C, Blasco González L, Sánchez Vañó R
J Pediatr Endocrinol Metab, 37(6):580-584, 26 Apr 2024
Cited by: 0 articles | PMID: 38661069
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Delphi consensus on the diagnosis and treatment of patients with short stature in Spain: GROW-SENS study.
Corripio-Collado R, Fernández-Ramos C, González-Casado I, Moreno-Macián F, López-Siguero JP, Labarta-Aizpún JI
J Endocrinol Invest, 45(4):887-897, 17 Nov 2021
Cited by: 0 articles | PMID: 34791604 | PMCID: PMC8918130
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A de novo CACNA1D missense mutation in a patient with congenital hyperinsulinism, primary hyperaldosteronism and hypotonia.
De Mingo Alemany MC, Mifsud Grau L, Moreno Macián F, Ferrer Lorente B, León Cariñena S
Channels (Austin), 14(1):175-180, 01 Dec 2020
Cited by: 19 articles | PMID: 32336187 | PMCID: PMC7219433
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Mutations in PMM2 gene in four unrelated Spanish families with polycystic kidney disease and hyperinsulinemic hypoglycemia.
Moreno Macián F, De Mingo Alemany C, León Cariñena S, Ortega López P, Rausell Felix D, Aparisi Navarro M, Martinez Matilla M, Cardona Gay C, Martinez Castellano F, Albiach Mesado V
J Pediatr Endocrinol Metab, 33(10):1283-1288, 25 Aug 2020
Cited by: 4 articles | PMID: 32841164
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Endocrinological late effects of oncologic treatment on survivors of medulloblastoma.
Hidalgo Santos AD, de Mingo Alemany MDC, Moreno Macián F, León Cariñena S, Collado Ballesteros E, Cañete Nieto A
Rev Chil Pediatr, 90(6):598-605, 01 Dec 2019
Cited by: 5 articles | PMID: 32186582
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What to consider when pseudohypoparathyroidism is ruled out: iPPSD and differential diagnosis.
Pereda A, Garin I, Spanish Network for Imprinting Disorders, Perez de Nanclares G
BMC Med Genet, 19(1):32, 02 Mar 2018
Cited by: 1 article | PMID: 29499646 | PMCID: PMC5834905
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A Novel Mutation of MAGEL2 in a Patient with Schaaf-Yang Syndrome and Hypopituitarism.
D Hidalgo-Santos A, Del Carmen DeMingo-Alemany M, Moreno-Macián F, Roselló M, Orellana C, Martínez F, Caro-Llopis A, León-Cariñena S, Tomás-Vila M
Int J Endocrinol Metab, 16(3):e67329, 01 Jul 2018
Cited by: 8 articles | PMID: 30323850 | PMCID: PMC6176277
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[Prophylactic thyroidectomy in RET proto-oncogen mutation].
Rodríguez Caraballo L, Gómez-Chacón Villalba J, Rodríguez Iglesias P, Cortés Sáez J, Moreno Macián F, Marco Macián A, Vila Carbó JJ
Cir Pediatr, 30(2):100-104, 20 Apr 2017
Cited by: 0 articles | PMID: 28857533
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The DATAC study: a new growth database. Description of the epidemiology, diagnosis and therapeutic attitude in a group of Spanish children with short stature.
Rodríguez Arnao MD, Sánchez AR, García-Rey C, Arroyo Díez FJ, Estrada RC, Cuartero BG, Merillas MA, López-Siguero JP, DATAC study group
J Pediatr Endocrinol Metab, 27(11-12):1201-1208, 01 Nov 2014
Cited by: 2 articles | PMID: 25210749
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Differentiated thyroid carcinoma in a girl with resistance to thyroid hormone management with triiodothyroacetic acid.
Ramos-Prol A, Antonia Pérez-Lázaro M, Isabel del Olmo-García M, León-de Zayas B, Moreno-Macián F, Navas-de Solis S, Merino-Torres JF
J Pediatr Endocrinol Metab, 26(1-2):133-136, 01 Jan 2013
Cited by: 8 articles | PMID: 23457315
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[Complete isosexual precocious puberty: clinical, pelvic ultrasound and laboratory features].
Moreno-Pérez O, Carles Genovés C, Moreno Macián F, Rius Peris J, Albiach Mesado V
An Pediatr (Barc), 69(5):413-419, 01 Nov 2008
Cited by: 0 articles | PMID: 19128741
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[Transient neonatal diabetes mellitus: a report of two cases].
Moreno Macián F, Carles Genovés C, Vargas F, Herráiz Pérez P, Verdeguer Bartual R, Albiach Mesado V
An Esp Pediatr, 51(1):87-88, 01 Jul 1999
Cited by: 0 articles | PMID: 10452157
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[Effectiveness of medical treatment of endocarditis due to Candida in premature newborns].
García Cantó E, Moreno Macián F, Gutiérrez Laso A, Alberola Pérez A, Sáez Palacios JM, Izquierdo Macián I, Morcillo Sopena F
An Esp Pediatr, 46(3):277-279, 01 Mar 1997
Cited by: 0 articles | PMID: 9173849
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1-14 of 14 results

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.

Use of [¹⁸F]fluorocholine PET/CT in the detection of primary hyperparathyroidism in paediatrics: a case report.

Delphi consensus on the diagnosis and treatment of patients with short stature in Spain: GROW-SENS study.

A de novo CACNA1D missense mutation in a patient with congenital hyperinsulinism, primary hyperaldosteronism and hypotonia.

Mutations in PMM2 gene in four unrelated Spanish families with polycystic kidney disease and hyperinsulinemic hypoglycemia.

Endocrinological late effects of oncologic treatment on survivors of medulloblastoma.

What to consider when pseudohypoparathyroidism is ruled out: iPPSD and differential diagnosis.

A Novel Mutation of MAGEL2 in a Patient with Schaaf-Yang Syndrome and Hypopituitarism.

[Prophylactic thyroidectomy in RET proto-oncogen mutation].

The DATAC study: a new growth database. Description of the epidemiology, diagnosis and therapeutic attitude in a group of Spanish children with short stature.

Differentiated thyroid carcinoma in a girl with resistance to thyroid hormone management with triiodothyroacetic acid.

[Complete isosexual precocious puberty: clinical, pelvic ultrasound and laboratory features].

[Transient neonatal diabetes mellitus: a report of two cases].

[Effectiveness of medical treatment of endocarditis due to Candida in premature newborns].

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