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Attend live and virtual events that provide a platform for education and collaborative discussion about the management of kidney disease and strategies to improve kidney health.
Any NephU member can request a presentation for their region or organization at no charge.
Over the past 50 years there has been significant advancement in Polycystic Kidney Disease (PKD) research which has allowed for the translation of these findings into not only an increased awareness of the disease but also improvements in clinical management.
Over the past 50 years there has been significant advancement in Polycystic Kidney Disease (PKD) research which has allowed for the translation of these findings into not only an increased awareness of the disease but also improvements in clinical management.
In this webinar, NephU speakers discuss the role of the pharmacist in neurocritical care. Clinical pharmacists significantly contribute to the care of patients with hyponatremia by identifying patients at risk and the source of hyponatremia, monitor serum sodium concentration and advise on the selection of appropriate therapeutic agent, dosage and duration.
In this webinar, NephU speakers discuss the role of the pharmacist in neurocritical care. Clinical pharmacists significantly contribute to the care of patients with hyponatremia by identifying patients at risk and the source of hyponatremia, monitor serum sodium concentration and advise on the selection of appropriate therapeutic agent, dosage and duration.
Home dialysis modalities are increasingly emphasized in healthcare payment models and represent an important patient-centric option for renal replacement therapy. Join us for this informational discussion with Dr Ankur Shah and Dr Natasha Dave on important strategies that can be employed to establish and grow a successful peritoneal dialysis program.
Home dialysis modalities are increasingly emphasized in healthcare payment models and represent an important patient-centric option for renal replacement therapy. Join us for this informational discussion with Dr Ankur Shah and Dr Natasha Dave on important strategies that can be employed to establish and grow a successful peritoneal dialysis program.
Join us for an international panel discussion featuring members from the IgAN Foundation, expert nephrologists, patients & caregivers. Panelists will discuss living with IgAN; highlighting the similarities and differences in each patient’s journey, identify how providers can support patients, facilitate the patients’ understanding of IgAN management, and identify the current gaps in management.
Join us for an international panel discussion featuring members from the IgAN Foundation, expert nephrologists, patients & caregivers. Panelists will discuss living with IgAN; highlighting the similarities and differences in each patient’s journey, identify how providers can support patients, facilitate the patients’ understanding of IgAN management, and identify the current gaps in management.
This presentation will examine the clinical overlap between CKD and major depressive disorder (MDD) in symptomatology, behavioral and biological mechanisms, the impact of comorbid depression on CKD outcomes, and strategies for effective management of depression in CKD.
In celebrating Black History Month, PsychU and NephU has invited, Dr. Napoleon Higgins to discuss the ongoing challenges that Black Americans face in the pursuit of equitable healthcare access and treatment.
Tune-in to the NephU webinar where we are joined by experts, Carl Bates, MD and Rannar Airik, PhD who will describe nephronophthisis (NPHP), the most frequent genetic cause for end-stage kidney disease in the first three decades of life, and its associated rare genetic syndromes such as Senior-Løken Syndrome (SLNS), Joubert Syndrome (JSRD), Meckel Syndrome (MKS), and Bardet-Biedl Syndrome (BBS).
Tune-in to the NephU webinar where we are joined by experts, Carl Bates, MD and Rannar Airik, PhD who will describe nephronophthisis (NPHP), the most frequent genetic cause for end-stage kidney disease in the first three decades of life, and its associated rare genetic syndromes such as Senior-Løken Syndrome (SLNS), Joubert Syndrome (JSRD), Meckel Syndrome (MKS), and Bardet-Biedl Syndrome (BBS).
