Results 91 to 100 of about 6,714 (210)
Renal tubular function in children and adolescents with Gitelnian's syndrome, the hypocalciuric variant of Bartter's syndrome [PDF]
, 2017 Renal tubular function was studied in 14 patients with Gitelman's syndrome and 14 control subjects. Apart from the biochemical hallmarks of Gitelman's syndrome, namely alkalaemia, hyperbi carbonataemia, hypokalaemia, hypomagnesaemia (with increased ...
Basilico, E. +5 more
core
Gitelman syndrome manifesting in early childhood and leading to delayed puberty: a case report
Journal of Medical Case Reports, 2012 Introduction Gitelman syndrome is an inherited autosomal recessive renal salt-wasting disorder. It presents with variable clinical symptoms including muscle weakness and fatigue, and the diagnosis is based on metabolic alkalosis, hypokalemia ...
Raza Farhan +4 more
doaj +1 more source
Criminal Behavior in Frontotemporal Dementia: A Multimodal MRI Study
Human Brain Mapping, Volume 46, Issue 11, 01 August 2025.Comparing patients with and without criminal behavior in frontotemporal dementia, structural brain alterations were found using various voxel‐, vertex‐, and region‐based approaches in the left temporal lobe (circular arranged). Criminal behavior was also associated with functional brain dysconnectivity between regions within the left temporal lobe and ...
Karsten Mueller +10 more
wiley +1 more source
Juxtaglomerular apparatus hyperplasia under dual angiotensin blockade. A footprint of adequate RAS inhibition or a concern for renal fibrosis? [PDF]
, 2012 Background: Dual renin-angiotensin system blockade with angiotensin-converting enzyme inhibitors and angiotensin receptor blockers has been advocated to minimize proteinuria. However, recent trials have questioned the renal safety of this approach.
Barat, Antonio +5 more
core +4 more sources
Type 1 diabetes presenting in adults: Trends, diagnostic challenges and unique features
Diabetes, Obesity and Metabolism, Volume 27, Issue S6, Page 57-68, August 2025.Abstract Type 1 diabetes (T1D) has been historically regarded as a childhood‐onset disease; however, recent epidemiological data indicate that adult‐onset T1D accounts for a substantial proportion of cases worldwide. There is evidence that adult‐onset T1D is associated with the classic T1D triad of elevated genetic risk, the presence of islet‐specific ...
Carmella Evans‐Molina, Richard A. Oram
wiley +1 more source
The role of the right temporoparietal junction in perceptual conflict: detection or resolution? [PDF]
, 2010 The right temporoparietal junction (rTPJ) is a polysensory cortical area that plays a key role in perception and awareness. Neuroimaging evidence shows activation of rTPJ in intersensory and sensorimotor conflict situations, but it remains unclear ...
A Maravita +78 more
core +1 more source
Caspian Journal of Reproductive Medicine, 2017 It is widely assumed that Gitelman syndrome is a rare genetic disorder with such electrolyte imbalance as hypokalemia and hypomagnesaemia. The impact of hypothyroidism on Gitelman syndrome and its management is not clear.
zahra kashi +3 more
doaj
A case of Gitelman's syndrome.
Nihon Naika Gakkai Zasshi, 1999 症例は20歳,女性.咽頭痛,発熱を主訴に受診した際,偶発的に著明な低K血症を指摘され,精査目的で入院した.経過中に下痢,嘔吐,口渇,多飲,多尿,テタニー,筋力低下等の症状を認めなかった.代謝性アルカローシスを伴う低K及び低Mg血症を認め尿中Ca/Cr(mol)比等からGitelman症候群と診断した.成人に認められる慢性の低K血症の診断に際しては, Gitelman症候群を念頭に置く必要があると考えた.
K, Kadomatsu +5 more
openaire +3 more sources
Arthritis &Rheumatology, Volume 77, Issue 5, Page 506-520, May 2025.Clinical tools that can aid in the diagnostic differentiation of juvenile dermatomyositis from muscular dystrophy.
Jacqueline A. Madison +9 more
wiley +1 more source