Results 251 to 260 of about 92,598 (348)

Mitochondrial Disease Diagnosed Following Preterm Birth at 29 Weeks of Gestation and Postpartum Heart Failure: A Case Report and Literature Review

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT In some cases, mitochondrial disease can remain undiagnosed until pregnancy reveals systemic symptoms. Clinicians should therefore consider this diagnosis in young patients presenting with diabetes, kidney disease, and hearing loss. Early diagnosis can improve maternal and fetal outcomes, particularly in high‐risk pregnancies complicated by ...
Tomoyuki Watanabe, Gen Ishikawa, Tsutomu Tabata   +2 more
wiley   +1 more source

Gallic acid alleviates hippocampus and cerebellum injuries in a rat model of hepatic encephalopathy. [PDF]

Sci Rep
Jafaripour L, Ahmadvand H, Babaeenezhad E, Esmaeilpour K, Maneshian M, Bashiri H, Asadi-Shekaari M.   +6 more
europepmc   +1 more source

An Overlooked Cause of Generalized Edema: A Case of Strongyloides stercoralis Hyperinfection Syndrome

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Strongyloides stercoralis infections are rare causes of protein‐losing enteropathy and must be considered in the differential diagnosis of patients who present with peripheral edema due to hypoproteinemia, especially in endemic countries. Stool routine examination in such individuals is a simple but essential way of identifying this organism.
Nyantakyi Adu‐Darko, Solomon Gyabaah, Aba Kwakomah Dapaah, Kwaku Asare‐Ankomah, Edna Naa Adaku Attuquaye, Esther Gyimah, Michael Odame Lartey, Yaw Ampem Amoako, Eileen Micah   +8 more
wiley   +1 more source

Overt hepatic encephalopathy after elective and preemptive TIPS: Risk factors and prognosis. [PDF]

JHEP Rep
Rudler M, Bouzbib C, Sultanik P, Roux C, Primard P, Jorus M, Kheloufi L, Weiss N, Meneghetti AR, Poussot B, Larrue H, Bureau C, Bedoya JU, Mouri S, Thabut D.   +14 more
europepmc   +1 more source

Lactitol versus lactulose in the treatment of chronic hepatic encephalopathy

, 1987
Marsha Y. Morgan, Katherine E. Hawley, Drago Stambuk   +2 more
openalex   +1 more source

Mitochondrial HMG‐CoA Synthase Deficiency Presenting as Pediatric Metabolic Stroke: A Case Report of a Novel Homozygous HMGCS2 (p.Ile56Asn) Variant

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Mitochondrial HMG‐CoA synthase deficiency should be suspected in infants with hypoketotic hypoglycemia, metabolic acidosis, and basal ganglia lesions. A 2‐year‐old boy with a novel HMGCS2 variant presented with refractory seizures and encephalopathy, highlighting the need for rapid metabolic and genetic evaluation for timely management.
Yasmeen Alshami, Osama Hroub, Mohammad Hroub, Saja Abouodeh, Zahra Makhamre, Ahmad G. Hammouri, Ibrahim Alzatari, Osama Atawneh   +7 more
wiley   +1 more source

Protective effects of synbiotic soymilk fortified with whey protein concentrate and zinc sulfate against bile duct ligated-induced hepatic encephalopathy.

, 2020
Yahya Jalilpiran‬, Nader Tanideh, Samane Rahmdel, Negar Azarpira, Maral Mokhtari, Zohreh Mazloom   +5 more
openalex   +1 more source

Implementing a Multidimensional Nursing Protocol in Dabie Bandavirus‐Induced SFTS With Critical Complications

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT This case demonstrates that a comprehensive, multidimensional nursing protocol—encompassing intensive monitoring, complication‐specific management, and rigorous infection control—is associated with favorable outcomes in this critically ill severe fever with thrombocytopenia syndrome (SFTS) patient with complex comorbidities like Parkinson's ...
Yongping Qiu, Minrui Li, Tingting Li, Jing Liu, Xiaodan Zhu, Shaoqin Zheng, Sha Yang   +6 more
wiley   +1 more source

Therapeutic Duel of Rifaximin Versus Lactulose in Hepatic Encephalopathy: A Systematic Review. [PDF]

Cureus
Oriko DO, Khawaj Z, Cheema MU, Talreja A, Tayyab MA, Zamir MH, Iqbal M, Farooq U, Ekomwereren O, Tariq MM, Hasan AH.   +10 more
europepmc   +1 more source