[Familial nanism with high levels of immunoreactive STH]

The diversity of the human hair colour assessed by visual scales and instrumental measurements. A worldwide survey.

International journal of cosmetic science·2016

Black hole physics. Black hole lightning due to particle acceleration at subhorizon scales.

Science (New York, N.Y.)·2014

[Short bowel syndrome cause of hypomagnesaemia importance of its diagnosis and treatment].

Nutricion hospitalaria·2014

[Percutaneous gastrostomy complicated with abdominal wall hematoma; severe anemia secondary to percutaneous endoscopic gastrostomy].

Nutricion hospitalaria·2012

Circulating free testosterone in obese men after bariatric surgery increases in parallel with insulin sensitivity.

Journal of endocrinological investigation·2012

Greying of the human hair: a worldwide survey, revisiting the '50' rule of thumb.

The British journal of dermatology·2012

Joint position paper on anterior ischemic optic neuropathy (AION). Vascular Risk Group and Systemic Autoimmune Diseases Group (GEAS) of the Spanish Society of Internal Medicine (SEMI) together with the Spanish Retina and Vitreous Society (SERV).

Revista clinica espanola·2026

Joint pain: a practical guide to the diagnosis of arthritis.

Revista clinica espanola·2026

Stickler syndrome type 1: case series and new genetic variants.

Revista clinica espanola·2026

Executive summary of the consensus document for recommendations on the treatment of venous thromboembolism in pregnancy: consensus document from the Spanish Society of Internal Medicine, the Spanish Society of Medical Radiology, the Spanish Society of Vascular Interventional Radiology and the Spanish Society of Gynecology and Obstetrics 2026.

Revista clinica espanola·2026

Treatment of osteoporosis in clinical practice: when, whom, how, and for how long.

Revista clinica espanola·2026

Metabolic alkalosis and clinical outcomes in acute heart failure: a systematic review and meta-analysis.

Revista clinica espanola·2026

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Pediatric blood & cancer·2026

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Frontiers in pediatrics·2026

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

European journal of human genetics : EJHG·2026

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Annals of medicine·2026

Familial short stature: genetic architecture, risk stratification, and precision management.

Frontiers in endocrinology·2026

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026

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[Familial nanism with high levels of immunoreactive STH]

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The diversity of the human hair colour assessed by visual scales and instrumental measurements. A worldwide survey.

Black hole physics. Black hole lightning due to particle acceleration at subhorizon scales.

[Short bowel syndrome cause of hypomagnesaemia importance of its diagnosis and treatment].

[Percutaneous gastrostomy complicated with abdominal wall hematoma; severe anemia secondary to percutaneous endoscopic gastrostomy].

Circulating free testosterone in obese men after bariatric surgery increases in parallel with insulin sensitivity.

Greying of the human hair: a worldwide survey, revisiting the '50' rule of thumb.

Joint position paper on anterior ischemic optic neuropathy (AION). Vascular Risk Group and Systemic Autoimmune Diseases Group (GEAS) of the Spanish Society of Internal Medicine (SEMI) together with the Spanish Retina and Vitreous Society (SERV).

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Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

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