person

Leonor L.

Country
Portugal
Department
Immunoallergology Department

Research Overview

Data & Insights

medical_services
Primary Speciality
Main therapeutic area

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Return Partnerships
Recurring site collaborations
0
Sites with multiple studies

Has run more than one trial at 0 of 48 partner sites.

Specializations

Allergic and Immunologic Disorders

The investigator focuses on conditions driven by immune dysregulation and allergen sensitization, addressing both cutaneous and respiratory manifestations.

  • Atopic Dermatitis
  • Allergic rhinoconjunctivitis
  • Chronic Inflammatory Demyelinating Polyneuropathy
  • Indolent Systemic Mastocytosis
  • Hidradenitis Suppurativa

Research integrates biologic therapies and targeted immunomodulators.

Hematologic and Oncology Therapeutics

Key interests include malignant hematologic diseases and solid tumours, emphasizing innovative treatment strategies.

  • Acute Myeloid Leukemia
  • Non‑small Cell Lung Cancer
  • Triple‑negative Breast Cancer
  • Follicular Lymphoma
  • Metastatic Head and Neck Squamous Cell Carcinoma

Efforts span immunotherapy, targeted agents, and precision medicine.

Cardiovascular and Metabolic Diseases

Investigation targets a spectrum of cardiovascular risk factors and metabolic disorders, aiming to reduce morbidity and mortality.

  • Atherosclerotic Cardiovascular Disease
  • Heart Failure with Reduced Ejection Fraction
  • Hypertension
  • Type 2 Diabetes
  • Severe Hypertriglyceridemia

Studies incorporate novel lipid‑lowering and cardioprotective agents.

Pulmonary and Respiratory Conditions

Research addresses chronic lung diseases and vascular pulmonary disorders, with emphasis on disease-modifying interventions.

  • Chronic Obstructive Pulmonary Disease
  • Idiopathic Pulmonary Fibrosis
  • Pulmonary Arterial Hypertension
  • Bronchiectasis
  • Asthma

Focus includes inhaled therapeutics and systemic agents.

Rare Genetic and Metabolic Disorders

The investigator contributes to the study of uncommon inherited diseases, exploring gene‑based and enzyme‑replacement approaches.

  • Alport Syndrome
  • Wilson Disease
  • Ornithine Transcarbamylase Deficiency
  • Classic Congenital Adrenal Hyperplasia
  • Hereditary Angioedema

Efforts aim to translate molecular insights into therapeutic options.

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