Results 81 to 90 of about 771,384 (234)
Altitude‐induced plasticity of respiratory central–peripheral chemoreflex interaction
The Journal of Physiology, EarlyView.Abstract figure legend Altitude‐induced plasticity of respiratory central–peripheral chemoreflex interaction. Seventeen participants completed modified rebreathing tests at low altitude and after 7–10 days of acclimatization at high altitude (3500 m). Central chemoreceptor activation was isolated using hypercapnic hyperoxia (end‐tidal PO2${{P}_{{{O}_2}}
Nasimi A. Guluzade +4 more
wiley +1 more source
Sporadic hypothyroidism-related hypokalemic paralysis: Diagnosis in a resource-poor setting
Journal of Family Medicine and Primary Care, 2017 Hypothyroidism and distal renal tubular acidosis causing hypokalemic paralysis (HP) have been described only in four female patients. HP as the initial manifestation of uncomplicated diabetes has been reported only in three young males.
Nadasha Kadeeja +3 more
doaj +1 more source
Acidosis tubular renal distal en dos niñas diagnosticadas de hipotiroidismo adquirido
Nefrología, 2018 Resumen: Se presentan dos casos en edad pediátrica diagnosticados de acidosis tubular renal (ATR) asociada a hipotiroidismo de causa autoinmune.El caso 1 desarrolló un íleo intestinal a los 5 años de edad en el seno de un problema respiratorio.
Norma E. Guerra-Hernández +4 more
doaj +1 more source
Renal tubular acidosis in childhood
Kidney International, 1981 A female infant, the product ofan uncomplicated full-term pregnancy in a 26-year-old primipara. was admitted to a local hospital at 26 days of age because of vomiting. Her weight stabilized at 3.0 kg and a relatively hyperosinolar formula, Baker's formula5, was prescribed.
openaire +2 more sources
A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy
Clinical Genetics, Volume 110, Issue 6, Page 736-741, December 2026.PIP5K1C‐related lethal congenital contracture syndrome with hyperinsulinism and optic atrophy. ABSTRACT Lethal congenital contracture syndrome 3 (LCCS3, MIM #611369) is a rare autosomal recessive neuromuscular disorder caused by biallelic loss‐of‐function (LOF) variants in PIP5K1C, reported in only two families to date.
Tameemi Abdalla Moady +3 more
wiley +1 more source
Renal tubular acidosis in primary Sjogren's syndrome
, 1992 Renal tubular acidosis (RTA) is a frequent extraglandular manifestation of Sjogren's syndrome; however, no distinction on the incidence of this renal tubular defect between primary and secondary Sjogren's syndrome has been reported.
Mavridis, A. A. +4 more
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A case of Sjogren’s syndrome presenting as hypokalaemia secondary to renal tubular acidosis [PDF]
Renal tubular acidosis (RTA) is a known but relatively rare presentation of Sjogren’s syndrome. It requires a high level of clinical suspicion to be diagnosed.
Murali, Sudhinder +3 more
core +1 more source
Clinical Case Reports, Volume 14, Issue 11, November 2026.ABSTRACT Hemophagocytic lymphohistiocytosis (HLH) is a life‐threatening hyperinflammatory syndrome with nonspecific clinical manifestations that can mimic common conditions in patients with alcohol dependence. Early clinical suspicion and rapid initiation of treatment are essential to prevent fatal outcomes.
Adalis Rivera +4 more
wiley +1 more source
Acute-onset paralysis in a patient of rheumatoid arthritis
Annals of Saudi Medicine, 2015 Renal tubular acidosis (RTA) is a disorder of renal acidification characterized by inability to acidify urine to pH
Ankur Nandan Varshney +3 more
doaj +1 more source
Lack of Pathogenic Mutation in the Human CAII Gene in an Individual Suffering Renal Tubular Acidosis [PDF]
, 2014 Renal tubular acidosis (RTA) is a rare genetic disorder. It has four clinical types, and type 3 demonstrates a mixed pattern of tubular dysfunction.
Shariati, Gholamreza +5 more
core +1 more source