Works matching DE "HYPOALDOSTERONISM"

Results: 118

Sotos Syndrome and Nephrocalcinosis a Rare But Possible Association Due to Impact on Contiguous Genes.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2025, v. 17, n. 2, p. 219, doi. 10.4274/jcrpe.galenos.2023.2023-3-11

By:

González-Rodríguez, Juan D.;
Inglés-Torres, Esther Q.;
Cabrera-Sevilla, José E.;
Ibáñez-Micó, Salvador;
Bermejo-Costa, Francisca;
Vera-Carbonell, Ascensión;
Bafalliu-Vidal, Juan A.;
Cortés-Mora, Pedro;
Lorente-Nicolás, Ana;
Donate-Legaz, José María

Publication type:

Article

Hyperkalaemia in diabetes: a silent risk predicting poor outcomes.

Published in:

Diabetic Medicine, 2018, v. 35, n. 8, p. 1049, doi. 10.1111/dme.13683

By:

Dojki, F. K.;
Bakris, G. L.

Publication type:

Article

Relative hypoaldosteronism in a patient with Wolcott-Rallison syndrome.

Published in:

Diabetic Medicine, 2016, v. 33, n. 3, p. e13, doi. 10.1111/dme.12968

By:

Uçar, A.;
Aydemir, Y.;
Doğan, A.;
Tunçez, E.

Publication type:

Article

Type IV RTA in Chronic Adrenal Insufficiency and Concomitant Lisinopril Treatment.

Published in:

Case Reports in Endocrinology, 2020, p. 1, doi. 10.1155/2020/8897112

By:

Galbiati, Francesca

Publication type:

Article

A Novel Mutation of the CYP11B2 in a Saudi Infant with Primary Hypoaldosteronism.

Published in:

Case Reports in Endocrinology, 2017, p. 1, doi. 10.1155/2017/8431475

By:

Alfaraidi, Lama;
Alfaifi, Abrar;
Alquaiz, Rawan;
Almijmaj, Faten;
Mawlawi, Horia

Publication type:

Article

Pseudohypoaldosteronism in a Neonate Presenting as Life-Threatening Hyperkalemia.

Published in:

Case Reports in Endocrinology, 2016, p. 1, doi. 10.1155/2016/6384697

By:

Attia, Najya A.;
Marzouk, Yousef I.

Publication type:

Article

Study of Adrenal Functions using ACTH stimulation test in Egyptian children with Sickle Cell Anemia: Correlation with Iron Overload.

Published in:

International Journal of Hematology-Oncology & Stem Cell Research, 2015, v. 9, n. 2, p. 6

By:

Hagag, Adel A.;
El-Farargy, Mohamed S.;
El-enein, Amany M. Abo

Publication type:

Article

Secondary pseudohypoaldosteronism caused by urinary tract infection associated with urinary tract abnormalities: case reports.

Published in:

Turkish Journal of Pediatrics, 2012, v. 54, n. 6, p. 682

By:

Sakallıoğlu, Onur

Publication type:

Article

Secondary pseudohypoaldosteronism caused by urinary tract infection associated with urinary tract anomalies: case reports.

Published in:

Turkish Journal of Pediatrics, 2012, v. 54, n. 1, p. 67

By:

Torum-Bayram, Meral;
Soylu, Alper;
Kasap-Demir, Belde;
Alaygut, Demet;
Türkmen, Mehmet;
Kavukçu, Salih

Publication type:

Article

Hypokalemic Periodic Paralysis Due To Distal Renal Tubular Acidosis.

Published in:

European Journal of General Medicine, 2015, p. 164, doi. 10.15197/sabad.1.12.33

By:

Gündüz, Ercan;
Zengin, Yılmaz;
Dursun, Recep;
İçer, Mustafa;
Güllü, Mehmet Nezir;
Durgun, Hasan Mansur

Publication type:

Article

Severe hyperkalemia is rescued by low-potassium diet in renal βENaC-deficient mice.

Published in:

Pflügers Archiv: European Journal of Physiology, 2017, v. 469, n. 10, p. 1387, doi. 10.1007/s00424-017-1990-2

By:

Boscardin, Emilie;
Perrier, Romain;
Sergi, Chloé;
Maillard, Marc;
Loffing, Johannes;
Loffing-Cueni, Dominique;
Koesters, Robert;
Rossier, Bernard;
Hummler, Edith

Publication type:

Article

A unifying mechanism for WNK kinase regulation of sodium-chloride cotransporter.

Published in:

Pflügers Archiv: European Journal of Physiology, 2015, v. 467, n. 11, p. 2235, doi. 10.1007/s00424-015-1708-2

By:

Huang, Chou-Long;
Cheng, Chih-Jen

Publication type:

Article

Parálisis periódica hipopotasémica asociada a acidosis tubular renal distal (tipo 1) e hipotiroidismo autoinmune.

Published in:

Revista Mexicana de Endocrinología, Metabolismo y Nutrición, 2018, v. 5, n. 2, p. 75

By:

MEREGILDO-RODRÍGUEZ, EDINSON DANTE;
FAILOC-ROJAS, VIRGILIO E.

Publication type:

Article

Use of renin angiotensin system inhibitors in patients with chronic kidney disease.

Published in:

Internal Medicine Journal, 2016, v. 46, n. 5, p. 626, doi. 10.1111/imj.13060

By:

Adam, W. R.;
Wright, J. R.

Publication type:

Article

Scholl solüsyonundaki sitrik aside bağlı gelişen Stevens-Johnson sendromu: Olgu sunumu

Published in:

Asthma Allergy Immunology / Astim Allerji Immunoloji, 2014, v. 12, n. 2, p. 110

By:

ÖZDEMİR, Öner;
UIMUS, Zeynep;
KIZMAZ, Didem;
ASLAN, Ebru

Publication type:

Article

Named Entity Recognition for Bacterial Type IV Secretion Systems.

Published in:

PLoS ONE, 2011, v. 6, n. 3, p. 1, doi. 10.1371/journal.pone.0014780

By:

Ananiadou, Sophia;
Sullivan, Dan;
Black, William;
Levow, Gina-Anne;
Gillespie, Joseph J.;
Mao, Chunhong;
Pyysalo, Sampo;
Kolluru, BalaKrishna;
Tsujii, Junichi;
Sobral, Bruno

Publication type:

Article

NR3C2 microdeletions—an underrecognized cause of pseudohypoaldosteronism type 1A: a case report and literature review.

Published in:

Laboratory Medicine, 2024, v. 5, n. 5, p. 640, doi. 10.1093/labmed/lmae005

By:

Boyanton, Bobby L;
Zarate, Yuri A;
Broadfoot, Brannon G;
Kelly, Thomas;
Crawford, Brendan D

Publication type:

Article

Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experience.

Published in:

Italian Journal of Pediatrics, 2016, v. 42, p. 1, doi. 10.1186/s13052-016-0282-3

By:

Bizzarri, Carla;
Olivini, Nicole;
Pedicelli, Stefania;
Marini, Romana;
Giannone, Germana;
Cambiaso, Paola;
Cappa, Marco

Publication type:

Article

Poster Sessions.

Published in:: Pediatric Diabetes, 2015, v. 16, p. 50, doi. 10.1111/pedi.12309
Publication type:: Article

TNF Lectin-Like Domain Restores Epithelial Sodium Channel Function in Frameshift Mutants Associated With Pseudohypoaldosteronism Type 1B.

Published in:

Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.00601

By:

Willam, Anita;
Aufy, Mohammed;
Tzotzos, Susan;
El-Malazi, Dina;
Poser, Franziska;
Wagner, Alina;
Unterköfler, Birgit;
Gurmani, Didja;
Martan, David;
Iqbal, Shahid Muhammad;
Fischer, Bernhard;
Fischer, Hendrik;
Pietschmann, Helmut;
Czikora, Istvan;
Lucas, Rudolf;
Lemmens-Gruber, Rosa;
Shabbir, Waheed

Publication type:

Article

The Authors' Reply: In systemic pseudohypoaldosteronism type 1 skin manifestations are not rare and the disease is not transient.

Published in:

2018

By:

Turan, Ihsan;
Topaloglu, Ali Kemal;
Yuksel, Bilgin

Publication type:

Letter to the Editor

In systemic pseudohypoaldosteronism type 1 skin manifestations are not rare and the disease is not transient.

Published in:

2018

By:

Hanukoglu, Aaron;
Hanukoglu, Israel

Publication type:

Letter to the Editor

Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance.

Published in:

Clinical Endocrinology, 2018, v. 88, n. 6, p. 799, doi. 10.1111/cen.13603

By:

Turan, Ihsan;
Kotan, Leman Damla;
Tastan, Mehmet;
Gurbuz, Fatih;
Topaloglu, Ali Kemal;
Yuksel, Bilgin

Publication type:

Article

Severe Hyponatremia in a 1-Week-Old Male Infant.

Published in:

2015

By:

Huebner, Karl;
Davis, T. Keefe;
Jackson, Tara;
Dawson, Jeffrey

Publication type:

Case Study

Carbonic Anhydrase II Deficiency in a Saudi Woman.

Published in:

Clinical Medicine Insights: Case Reports, 2015, n. 8, p. 7, doi. 10.4137/CCRep.S16897

By:

Alhuzaim, Omar N.;
Almohareb, Ohoud M.;
Sherbeeni, Safiya M.

Publication type:

Article

A rare case of persistent hyperkalaemia.

Published in:

2021

By:

Lewis, Thomas;
Roberts, Gareth;
Zouwail, Soha

Publication type:

Case Study

Regional anesthesia is safe and effective for lower limb orthopedic surgery in patient with renal tubular acidosis and hypokalemia.

Published in:

2018

By:

Gurajala, Indira;
Annaji Nikhar, Sapna;
Jayaram, Kavitha;
Gopinath, Ramachandran

Publication type:

Case Study

Elements.

Published in:

QJM: An International Journal of Medicine, 2012, v. 105, n. 9, p. 811, doi. 10.1093/qjmed/hcs167

By:

Bannon, Michael

Publication type:

Article

Tropical distal renal tubular acidosis: clinical and epidemiological studies in 78 patients.

Published in:

QJM: An International Journal of Medicine, 2012, v. 105, n. 9, p. 861, doi. 10.1093/qjmed/hcs139

By:

Khositseth, S.;
Bruce, L.J.;
Walsh, S.B.;
Bawazir, W.M.;
Ogle, G.D.;
Unwin, R.J.;
Thong, M.-K.;
Sinha, R.;
Choo, K.E.;
Chartapisak, W.;
Kingwatanakul, P.;
Sumboonnanonda, A.;
Vasuvattakul, S.;
Yenchitsomanus, P.;
Wrong, O.

Publication type:

Article

Back to the future: renal tubular acidosis then and now.

Published in:

QJM: An International Journal of Medicine, 2012, v. 105, n. 9, p. 915, doi. 10.1093/qjmed/hcs134

By:

Unwin, Robert J.

Publication type:

Article

Phylogenomics and sequence-structure-function relationships in the GmrSD family of Type IV restriction enzymes.

Published in:

BMC Bioinformatics, 2015, v. 16, p. 1, doi. 10.1186/s12859-015-0773-z

By:

Machnicka, Magdalena A.;
Kaminska, Katarzyna H.;
Dunin-Horkawicz, Stanislaw;
Bujnicki, Janusz M.

Publication type:

Article

A Japanese girl with aldosterone synthase deficiency requiring fludrocortisone until 10 years of age.

Published in:

2023

By:

Koyama, Satomi;
Tsuboi, Tatsuo;
Naganuma, Junko;
Arisaka, Osamu;
Yoshihara, Shigemi

Publication type:

Case Study

Neonatal renal venous thrombosis followed by secondary pseudohypoaldosteronism.

Published in:

Pediatrics International, 2012, v. 54, n. 6, p. 936, doi. 10.1111/j.1442-200X.2012.03617.x

By:

Nakashima, Hideyuki;
Kibe, Tetsuya;
Ohro, Yoichiro;
Fujita, Naoya

Publication type:

Article

Autosomal Dominant Pseudohypoaldosteronism Type 1 in an Infant with Salt Wasting Crisis Associated with Urinary Tract Infection and Obstructive Uropathy.

Published in:

Case Reports in Endocrinology, 2013, p. 1, doi. 10.1155/2013/524647

By:

Bowden, Sasigarn A.;
Cozzi, Corin;
Hickey, Scott E.;
Thrush, Devon Lamb;
Astbury, Caroline;
Nuthakki, Sushma

Publication type:

Article

Clinical and laboratory characteristics of salivary gland ultrasonography‐positive patients with primary Sjögren's syndrome.

Published in:

Oral Diseases, 2025, v. 31, n. 1, p. 239, doi. 10.1111/odi.15051

By:

Yang, Yan;
Cheng, Lian;
Qin, Ai‐Ping;
Xu, Jun

Publication type:

Article

CME-Labor 23.

Published in:

Praxis (16618157), 2011, v. 100, n. 25, p. 1523, doi. 10.1024/1661-8157/a000746

By:

Saleh, Lanja

Publication type:

Article

Pseudohypoaldosteronism type 1 and Liddle's syndrome mutations that affect the single-channel properties of the epithelial Na<sup>+</sup> channel.

Published in:

Physiological Reports, 2015, v. 3, n. 11, p. 1, doi. 10.14814/phy2.12600

By:

Boiko, Nina;
Kucher, Volodymyr;
Stockand, James D.

Publication type:

Article

ARC Syndrome; Arthrogryposis, Renal and Cholestasis.

Published in:

Medical Journal of Tabriz University of Medical Sciences & Health Services, 2013, v. 35, n. 2, p. 106

By:

Malaki, Majid;
Malekian, Armen;
Rafeey, Mandana;
Azarafar, Anoush

Publication type:

Article

A novel mutation in exon 9 of Cullin 3 gene contributes to aberrant splicing in pseudohypoaldosteronism type II.

Published in:

FEBS Open Bio, 2018, v. 8, n. 3, p. 461, doi. 10.1002/2211-5463.12389

By:

Shao, Leping;
Cui, Li;
Lu, Jingru;
Lang, Yanhua;
Bottillo, Irene;
Zhao, Xiangzhong

Publication type:

Article

Identification of a Novel CYP11B2 Variant in a Family with Varying Degrees of Aldosterone Synthase Deficiency.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2024, v. 16, n. 1, p. 95, doi. 10.4274/jcrpe.galenos.2022.2022-3-4

By:

Garrelfs, Mark R.;
Rinne, Tuula;
Hillebrand, Jacquelien J.;
Lauffer, Peter;
Bijlsma, Merijn W.;
der Grinten, Hedi L. Claahsen-van;
de Leeuw, Nicole;
Finken, Martijn J. J.;
Rotteveel, Joost;
Zwaveling-Soonawala, Nitash;
Nieuwdorp, Max;
van Trotsenburg, A. S. Paul;
Mooij, Christiaan F.

Publication type:

Article

Nephrogenic Syndrome of Inappropriate Antidiuresis Mimicking Hyporeninemic Hypoaldosteronism: Case Report of Two Infants.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 2, p. 214, doi. 10.4274/jcrpe.galenos.2021.2021.0191

By:

Mammadova, Jamala;
Kara, Cengiz;
Bitkin, Eda Çelebi;
Güllü, Elif İzci;
Aydın, Murat

Publication type:

Article

Clinical Management in Systemic Type Pseudohypoaldosteronism Due to SCNN1B Variant and Literature Review.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 4, p. 446, doi. 10.4274/jcrpe.galenos.2020.2020.0107

By:

Küçükali, Gülin Karacan;
Çetinkaya, Semra;
Tunç, Gaffari;
Oğuz, M. Melek;
Çelik, Nurullah;
Akkaş, Kardelen Yağmur;
Şenel, Saliha;
Lafcı, Naz Güleray;
Erdeve, Şenay Savaş

Publication type:

Article

Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 2, p. 232, doi. 10.4274/jcrpe.galenos.2020.2019.0216

By:

Turan, Hande;
Çakır, Aydilek Dağdeviren;
Özer, Yavuz;
Tarçın, Gürkan;
Özcabi, Bahar;
Ceylaner, Serdar;
Ercan, Oya;
Evliyaoğlu, Saadet Olcay

Publication type:

Article

Dermal and Ophthalmic Findings in Pseudohypoaldosteronism.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, n. 2, p. 155, doi. 10.4274/jcrpe.1740

By:

Korkut, Sabriye;
Gökalp, Emir;
Özdemir, Ahmet;
Kurtoğlu, Selim;
Demirtaş, Şafak;
Gül, Ülkü;
Baştuğ, Osman

Publication type:

Article

Acquired Proximal Renal Tubular Dysfunction in 9 Labrador Retrievers with Copper-Associated Hepatitis (2006-2012).

Published in:

Journal of Veterinary Internal Medicine, 2013, v. 27, n. 3, p. 491, doi. 10.1111/jvim.12065

By:

Langlois, D.K.;
Smedley, R.C.;
Schall, W.D.;
Kruger, J.M.

Publication type:

Article

Molecular Analysis of the CYP11B2 Gene in 62 Patients with Hypoaldosteronism Due to Aldosterone Synthase Deficiency.

Published in:

2021

By:

Merakou, Christina;
Fylaktou, Irene;
Sertedaki, Amalia;
Dracopoulou, Maria;
Voutetakis, Antonis;
Efthymiadou, Alexandra;
Christoforidis, Athanasios;
Dacou-Voutetakis, Catherine;
Chrysis, Dionisios;
Kanaka-Gantenbein, Christina

Publication type:

journal article

Hypokalaemic Periodic Paralysis with Renal Tubular Acidosis in Patients with Primary Sjögren's Syndrome Presenting as Quadriparesis and Recurrent Paraparesis.

Published in:

Journal of the Indian Academy of Clinical Medicine, 2023, v. 24, n. 2, p. 155

By:

Sarna, Mukesh Kumar;
Parakh, Rishabh;
Shah, Sarthak;
Setia, Mansi;
Pahadia, Manish;
Sarna, Sudha

Publication type:

Article

Wilson's Disease Presents as Recurrent Hypokalemic Muscle Paralysis.

Published in:

Indian Journal of Nephrology, 2023, v. 33, n. 4, p. 292, doi. 10.4103/ijn.ijn_143_22

By:

Shankar, Mythri;
Nayaka, Monica;
Aralapuram, Kishan;
Gurusiddaiah, Sreedhara C.

Publication type:

Article

Hyperkalemia unveiled: A case of Barakat syndrome.

Published in:

Indian Journal of Nephrology, 2020, v. 30, n. 2, p. 135, doi. 10.4103/ijn.IJN_132_19

By:

Singh, Kulwant;
Sethi, Jasmine;
Bhargava, Vinant

Publication type:

Article

Post-Renal Transplant Metabolic Acidosis: A Neglected Entity.

Published in:

Indian Journal of Nephrology, 2019, v. 29, n. 2, p. 116, doi. 10.4103/ijn.IJN_93_18

By:

Fernando, M. E.;
Jayanivash, J.;
Srinivasaprasad, N. D.;
Suren, S.;
Thirumalvalavan, K.

Publication type:

Article