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Publications by Noemi Vidal-Folch

A Tailored Approach to Fusion Transcript Identification Increases Diagnosis of Rare Inherited Disease

Multidisciplinary

English

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Approach to Inherited Cystic Kidney Disease

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Identification of a Novel RUNX1-TACC1 Fusion Transcript in Acute Myeloid Leukaemia

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Erratum To: Chronic Obstructive Pulmonary Disease Individualized Therapy: Tailored Approach to Symptom Management

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Identification of a Novel NUP98-RARA Fusion Transcript as the 14th Variant of Acute Promyelocytic Leukemia

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Identification of a Rare E6a2 BCR-ABL Fusion Gene During the Disease Progression of Chronic Myelomonocytic Leukemia: A Case Report

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Whipple´s Disease, a Rare Malabsorption Syndrome of Late Diagnosis

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Inherited Real Risk of Alzheimer's Disease: Bedside Diagnosis and Primary Prevention

Frontiers in Aging Neuroscience

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Renovascular Disease. A Contemporary Approach to the Diagnosis and Treatment

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Commentary to "A Tailored Surgical Approach to the Palpable Undescended Testis"

Journal of Pediatric Urology

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