Aller au contenu principal
Profil bibliographique

Karin Tran‐Lundmark

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

86Publications signalées
1517Citations signalées
3Affiliations récentes

Les institutions déclarées

Les domaines associés

Pulmonary Hypertension Research and TreatmentsProteoglycans and glycosaminoglycans researchCell Adhesion Molecules ResearchTransplantation: Methods and OutcomesProtease and Inhibitor Mechanisms

Les publications récentes

Accès ouvert 2026 article OpenAlex

Risk factors for posttransplant lymphoproliferative disorder (PTLD) in pediatric heart recipients were associated with impairment of the immune system – a multicenter study from Sweden

Britt‐Marie Ekman‐Joelsson, Michal Odermarsky, Karin Tran‐Lundmark, Maria Sjöborg Alpman et autres

Background: Posttransplant lymphoproliferative disorder (PTLD) is a potentially lethal complication after pediatric heart transplantation (PHT). We have previously reported an association between PTLD and (1) sternotomy during infancy, (2) mismatch concerning Epstein-Barr virus infection, (3) hypoplastic left ventricle and (4) surgically palliated …

se (code pays fourni par la source)

0 citations JHLT Open
Accès ouvert 2026 article OpenAlex

Histology-guided 3D virtual staining of microCT-imaged lung tissue via deep learning

Cristina Almagro-Pérez, Niccolò Peruzzi, Csaba Galambos, Andrew H. Song et autres

Histologically stained tissue sections are considered the gold standard for studying microscopic anatomy and diagnosing disease in clinical practice. However, the processes of sectioning and staining are laborious, and the overall method relies on two-dimensional analysis. In contrast, X-ray-based virtual histology offers …

ch, se, us (code pays fourni par la source)

2 citations Journal of The Royal Society Interface
Accès ouvert 2026 article OpenAlex

Hypoxia Induces Adaptive Lymphangiogenesis via Cd74 and Vegfr3 to Modulate Pulmonary Hypertension

M Moss, Timothy Klouda, Y Li, Ying Liu et autres

BACKGROUND: Pulmonary arterial hypertension (PAH) is characterized by excessive remodeling of the distal arterioles and arteries, driven by endothelial cell (EC) apoptosis and uncontrolled mural cell proliferation. Increasing evidence suggests immune dysregulation in PAH, but one crucial part of the immune system, …

us, se (code pays fourni par la source)

0 citations Circulation Research
2026 article OpenAlex

Recent advances in the clinical management of end-stage pediatric pulmonary hypertension

Oscar van der Have, Rachel K. Hopper, Rebecca J. Kameny, Karin Tran‐Lundmark

PURPOSE OF REVIEW: This review aims to give an overview of recent advances in the clinical management of children <18 years of age with end-stage pulmonary hypertension refractory to conventional medical therapy. RECENT FINDINGS/SUMMARY: The increased awareness and characterization of pediatric pulmonary …

se, us (code pays fourni par la source)

0 citations Current Opinion in Pulmonary Medicine
Accès ouvert 2026 article OpenAlex

The Nordic Experience of Pediatric Heart‐Lung Transplantation

Oscar van der Have, Michal Odermarsky, Thomas Möller, Klaus Juul et autres

BACKGROUND: Pediatric heart-lung transplantation (pHLTx) remains the only treatment option for children with significant and fixed elevation of pulmonary vascular resistance (PVR) in the setting of uncorrectable end-stage heart disease. We aimed to determine the characteristics, waiting list course and long-term outcomes …

se, no, dk, fi (code pays fourni par la source)

0 citations Clinical Transplantation
2026 preprint OpenAlex

Efficient murine cardiac phenotyping by combining synchrotron-based phase-contrast micro-CT, histology, immunofluorescence and spatial transcriptomics

Niccolò Peruzzi, Ayse Ceren Mutgan, Kinga I. Gawlik, Timothy J. Mead et autres

1. Abstract Congenital heart disease is commonly studied using genetically modified mouse models, but characterization of complex three-dimensional (3D) cardiac anomalies remains technically challenging. Histology of fixed paraffin-embedded samples, typically used for structural and molecular analysis, is limited to two dimensions (2D). …

se, us, ch (code pays fourni par la source)

0 citations bioRxiv (Cold Spring Harbor Laboratory)
Accès ouvert 2026 article OpenAlex

Current availability and status of paediatric cardiac transplantation and mechanical circulatory support in twenty-eight European countries

Oscar van der Have, Esme Dunne, Karin Tran‐Lundmark, Julie Wacker et autres

We sought to investigate the inter- and intra-country variation in paediatric heart transplantation (HTx) and mechanical circulatory support (MCS) availability and practice in Europe. Data was obtained through a survey circulated to paediatric transplant cardiologists identified through the Association of European Paediatric …

se, ie, ch, us, at, cz, de, be, is, nl, hr, si, lv, tr, it, dk, ba, pt, pl, fi, hu, ro, sk, gb, no, fr (code pays fourni par la source)

0 citations European Journal of Pediatrics
Accès ouvert 2025 article OpenAlex

Protein-losing enteropathy following Fontan completion: A 30-year national cohort study in Sweden

Mikaela Dolk, Indra Schütz, Erik Herou, Felicia Nordenstam et autres

OBJECTIVE: To characterize patients with protein-losing enteropathy (PLE) diagnosed before age 18 years within a nationwide Swedish Fontan cohort. METHODS: Surgical records and medical charts were reviewed for all patients born after January 1, 1993, who underwent Fontan completion before January 1, …

se (code pays fourni par la source)

1 citation Journal of Thoracic and Cardiovascular Surgery
2025 conference-abstract OpenAlex

Abstract 4363073: Somatic activating mutation in Phosphoinositide 3-kinase in a plexiform lesion of a patient with hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension

Katharina Schimmel, Evon DeBose-Scarlett, Yue Qi, Serena Y. Tan et autres

Background: Hereditary hemorrhagic telangiectasia (HHT) and hereditary pulmonary arterial hypertension (HPAH) are genetic diseases that affect the pulmonary vasculature. HHT and HPAH are due to a haploinsufficiency in components of the bone morphogenetic protein receptor type 2 (BMPR2) pathway. Despite shared genetics, …

us, se (code pays fourni par la source)

0 citations Circulation
Accès ouvert 2025 article OpenAlex

Exploring the Impact of Platelet‐Derived Growth Factor D in Pulmonary Hypertension Development

Philip Tannenberg, Karin Tran‐Lundmark, Ya‐Ting Chang, Hanna Gladh et autres

ABSTRACT Pulmonary arterial hypertension (PAH) is a life‐threatening condition with no cure, making research into its underlying mechanisms critical. The platelet‐derived growth factor (PDGF) signaling pathway plays a crucial role in vascular remodeling, a key factor in PAH progression. Anti‐PDGF receptor therapies, …

se, tw (code pays fourni par la source)

0 citations Pulmonary Circulation

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.