Results 211 to 220 of about 15,555 (263)

Restrictive Cardiomyopathy

, 2007
James T. Willerson, L. Maximilian Buja, John Goodwin   +2 more
openaire   +2 more sources

Mechanical circulatory support bridge for restrictive cardiomyopathy with biventricular and pulmonary failure to cardiac transplantation. [PDF]

Indian J Thorac Cardiovasc Surg
Sainathan S, Mulinari L.
europepmc   +1 more source

Differentiation of constrictive pericarditis from restrictive cardiomyopathy using mitral annular velocity by tissue Doppler echocardiography

, 2004
Jong‐Won Ha, Steve R. Ommen, A. Jamil Tajik, Marion E. Barnes, Naser M. Ammash, Morie A. Gertz, James B. Seward, Jae K. Oh   +7 more
openalex   +2 more sources

Brentuximab Vedotin With Adriamycin, Vinblastine, and Dacarbazine for Patients Aged 18–59 Years With Untreated Advanced Stage Classical Hodgkin Lymphoma: The Largest Real‐Life Series From Southern Italy Cancer Centers

European Journal of Haematology, Volume 116, Issue 2, Page 174-184, February 2026.
ABSTRACT BV + AVD is increasingly used for frontline treatment of stage III/IV cHL. Young adults and adults (Ya&A) were the most common patients treated with BV + AVD in clinical trials but have not been studied in non‐trial settings. We conducted a real‐life study in secondary and tertiary cancer centers to evaluate the PFS in 18–59 years aged ...
Marco Picardi, Annamaria Vincenzi, Claudia Giordano, Novella Pugliese, Alessia Scarpa, Assunta Lombardi, Elena Vigliar, Giancarlo Troncone, Rosaria Cappiello, Massimo Mascolo, Giovanni Esposito, Maria Prastaro, Ciro Santoro, Roberta Esposito, Carlo Gabriele Tocchetti, Ciro Mainolfi, Rosa Fonti, Silvana Del Vecchio, Fabio Trastulli, Mario Annunziata, Rossella Iula, Catello Califano, Marianna Carchia, Marcello Persico, Alessia Salemme, Emanuele Nicolai, Andrea Soricelli, Marco Salvatore, Fabrizio Pane   +28 more
wiley   +1 more source

Biallelic potential disease-causing missense variants in TAF1A in two siblings with infantile restrictive cardiomyopathy. [PDF]

Eur J Med Genet
Jiang N, Xu W, Abdelhakim A, Matveyenko A, Szabolcs M, Copeland WC, Disco M, Iglesias A, Lee TM, Naini A, Ganapathi M.   +10 more
europepmc   +1 more source

Interdisciplinary Approach in Pediatric Patients With Recessive Dystrophic Epidermolysis Bullosa: Experience From the Dermatology Service and the Palliative Care and Complex Chronic Patient Team at Sant Joan de Déu Hospital (Barcelona, Spain)

Journal of Evaluation in Clinical Practice, Volume 32, Issue 1, February 2026.
ABSTRACT Background and Aims Epidermolysis bullosa is a rare genetic disorder causing extreme mucocutaneous fragility, requiring specialized, multidisciplinary care. Integrating palliative care into Epidermolysis bullosa management has proven beneficial in symptom control and psychosocial support.
Juan Manuel Martínez‐Ripoll, Marta García‐Domingo, Yolanda M. De la Fuente Robles   +2 more
wiley   +1 more source

The bird hunting story: constrictive pericarditis and restrictive cardiomyopathy. [PDF]

Indian J Thorac Cardiovasc Surg
Subramaniam KG, Sharma D.
europepmc   +1 more source

The Effectiveness of Family Health Conversations Delivered by Nurses: A Systematic Review

Journal of Clinical Nursing, Volume 35, Issue 2, Page 539-564, February 2026.
ABSTRACT Aim To extract and interpret quantitative data exploring the effectiveness of family health conversations (FHCs) on family functioning, perceived support, health‐related quality of life, caregiver burden and family health in families living with critical or chronic health conditions.
Birte Østergaard, Erla Kolbrun‐Svavarsdottir, Anne Brødsgaard, Stine Rosenstrøm, Cristina Garcia‐Vivar, Hanne Konradsen, Karin Brochstedt‐Dieperink, Lorenz Imhof, Romy Mahrer‐Imhof, Marie Louise Luttik   +9 more
wiley   +1 more source

The impact of Hnrnpl deficiency on transcriptional patterns of developing muscle cells

FEBS Open Bio, Volume 16, Issue 1, Page 178-198, January 2026.
We performed nanopore whole‐transcriptome sequencing comparing RNA from Hnrnpl‐knockdown versus control C2C12 myoblasts to investigate the contributions of Hnrnpl to muscle development. Our results indicate that Hnrnpl regulates the expression of genes involved with Notch signaling and skeletal muscle, particularly splicing patterns of specific muscle ...
Hannah R. Littel, Mekala Gunasekaran, Audrey L. Daugherty, Natalya M. Wells, Johnnie Turner, Christine C. Bruels, Christina A. Pacak, Isabelle Draper, Peter B. Kang   +8 more
wiley   +1 more source

Mutations in the TCAP gene may lead to restrictive phenotype hypertrophic cardiomyopathy with poor prognosis: case report [PDF]

Yunwen Hu, Guangzhong Liu, Jie Yuan, Da Yin, Yaowang Lin   +4 more
openalex   +1 more source