[Peutz-Jeghers syndrome, apropos of a case]

Results of a survey about specific inflammatory bowel disease units in Andalusia.

Revista espanola de enfermedades digestivas·2009

[A high-resolution gastroenterology clinic in Andalusia: what is it, and how should it work].

Revista espanola de enfermedades digestivas·2008

[Pyoderma gangrenosum with an atypical location and a rapid response to cyclosporin A].

Gastroenterologia y hepatologia·1999

[Chronic hereditary pancreatitis].

Revista espanola de enfermedades digestivas·1994

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

Pulmonary embolism: what does the new AHA/ACC 2026 guide add.

Revista clinica espanola·2026

Training in internal medicine in the age of artificial intelligence.

Revista clinica espanola·2026

Beyond the Rash: Simultaneous Bilateral Facial Nerve Palsy Following Childhood Varicella Infection.

Clinical case reports·2026

Successful treatment of refractory classic juvenile pityriasis rubra pilaris with adalimumab in a 4-year-old girl: a case report.

Frontiers in immunology·2026

Retrospective Analysis of Paenibacillus urinalis Cultures Primarily Obtained from Sterile Sites in a Pediatric Population from Turkey.

Microorganisms·2026

A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL.

Genes·2026

Never Say Never: Presumed Inherited Factor VII Deficiency Lies in Wait for 17 Years.

Cureus·2026

Simultaneous Bilateral Tibial Tubercle Avulsion Fractures Complicated by Compartment Syndrome in an Adolescent With Osteogenesis Imperfecta: A Case Report.

Case reports in orthopedics·2026

Related Experiment Videos

[Peutz-Jeghers syndrome, apropos of a case]

Related Concept Videos

Results of a survey about specific inflammatory bowel disease units in Andalusia.

[A high-resolution gastroenterology clinic in Andalusia: what is it, and how should it work].

[Pyoderma gangrenosum with an atypical location and a rapid response to cyclosporin A].

[Chronic hereditary pancreatitis].

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

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

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

Pulmonary embolism: what does the new AHA/ACC 2026 guide add.

Training in internal medicine in the age of artificial intelligence.

Beyond the Rash: Simultaneous Bilateral Facial Nerve Palsy Following Childhood Varicella Infection.

Successful treatment of refractory classic juvenile pityriasis rubra pilaris with adalimumab in a 4-year-old girl: a case report.

Retrospective Analysis of Paenibacillus urinalis Cultures Primarily Obtained from Sterile Sites in a Pediatric Population from Turkey.

A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL.

Never Say Never: Presumed Inherited Factor VII Deficiency Lies in Wait for 17 Years.

Simultaneous Bilateral Tibial Tubercle Avulsion Fractures Complicated by Compartment Syndrome in an Adolescent With Osteogenesis Imperfecta: A Case Report.

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