Cargando…

Challenges in the diagnosis and management of Pseudohypoaldosteronism Type 1

Detalles Bibliográficos
Autores principales:	Visser, Uma, Jenkins, Paul, Lafferty, Tony
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428644/ http://dx.doi.org/10.1186/1687-9856-2015-S1-P126

Ejemplares similares

Pseudohypoaldosteronism type 1: clinical features and management in infancy
por: Amin, N, et al.
Publicado: (2013)

Critical Points in the Management of Pseudohypoaldosteronism Type 1
por: Güran, Tülay, et al.
Publicado: (2011)

Hypercalcemia in an Infant With Pseudohypoaldosteronism Type 1
por: Jeng, Henry, et al.
Publicado: (2021)

Neonatal Pseudohypoaldosteronism Type-1 in Japan
por: Fujioka, Kazumichi, et al.
Publicado: (2022)

Challenges of Diagnosing Pseudohypoaldosteronism (PHA) in an Infant
por: Babar, Ghufran Saeed, et al.
Publicado: (2022)

Clinical features and molecular basis of pseudohypoaldosteronism type 1
por: Tajima, Toshihiro, et al.
Publicado: (2017)

Systemic pseudohypoaldosteronism-1 with episodic dyslipidemia in a Sudanese child
por: Abdalla, Asmahan, et al.
Publicado: (2021)

Does Pseudohypoaldosteronism Mask the Diagnosis of Congenital Adrenal Hyperplasia?
por: Ağladıoğlu, Sebahat Yılmaz, et al.
Publicado: (2011)

Pseudohypoaldosteronism in a neonate presenting as life-threatening arrhythmia
por: Rajpoot, Sudeep K, et al.
Publicado: (2014)

Dermal and Ophthalmic Findings in Pseudohypoaldosteronism
por: Korkut, Sabriye, et al.
Publicado: (2015)

Clinical Management in Systemic Type Pseudohypoaldosteronism Due to SCNN1B Variant and Literature Review
por: Karacan Küçükali, Gülin, et al.
Publicado: (2021)

MON-373 Pseudohypoaldosteronism Type 1, a Masquerader: Case Study
por: Akinseye, Leah, et al.
Publicado: (2019)

Pseudohypoaldosteronism Type 1: A Rare Cause of Severe Dyselectrolytemia and Cardiovascular Collapse in Neonates
por: Saravanapandian, Namasivayam, et al.
Publicado: (2012)

A girl with primary pigmented adrenocortical disease (PPNAD): challenges in diagnosis and management
por: Wejaphikul, Karn, et al.
Publicado: (2013)

Novel Mutations in the SCNN1A Gene Causing Pseudohypoaldosteronism Type 1
por: Wang, Jian, et al.
Publicado: (2013)

Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene
por: Nobel, Yael R, et al.
Publicado: (2016)

A Rare Case of Pseudohypoaldosteronism Type II or Gordon Syndrome
por: Manas, F N U, et al.
Publicado: (2021)

A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene
por: Lee, Se Eun, et al.
Publicado: (2011)

Pseudohypoaldosteronism: case report and discussion of the syndrome.
por: Throckmorton, D. C., et al.
Publicado: (1991)

Acid–Base Imbalance in Pseudohypoaldosteronism Type 1 in Comparison With Type IV Renal Tubular Acidosis
por: Adachi, Masanori, et al.
Publicado: (2022)

Systemic Pseudohypoaldosteronism Type I: A Case Report and Review of the Literature
por: Nur, Nasifa, et al.
Publicado: (2017)

Salt-Losing Syndrome in a Girl with Type I and II Pseudohypoaldosteronism
por: Szmigielska, Agnieszka
Publicado: (2022)

Rare Cause of Hyperkalemia in the Newborn Period: Report of Two Cases of Pseudohypoaldosteronism Type 1
por: Manipriya, R., et al.
Publicado: (2018)

A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population
por: Alzahrani, Ali S, et al.
Publicado: (2021)

Pseudohypoaldosteronism Type 1 (arPHA1) Treated With Sodium Polystyrene Sulfonate Pretreated Milk
por: Khalil, Syed Tariq, et al.
Publicado: (2015)

Transient Pseudohypoaldosteronism in an Infant: A Case Report
por: Latt, Tin Nwe, et al.
Publicado: (2018)

“Brucellupus” in a boy: challenging sle diagnosis in childhood
por: Paganelli, Valeria, et al.
Publicado: (2014)

A young child with pseudohypoaldosteronism type II by a mutation of Cullin 3
por: Tsuji, Shoji, et al.
Publicado: (2013)

Phenotypic variation of autosomal recessive pseudohypoaldosteronism type I: a case in point
por: Kala Ahluwalia, Gunjeet, et al.
Publicado: (2014)

Pseudohypoaldosteronism Type II Caused by CUL3 Mutation Presented with Visual Impairment
por: Wang, Qiao, et al.
Publicado: (2018)

Errate: Salt-Losing Syndrome in a Girl with Type I and II Pseudohypoaldosteronism
por: Szmigielska, Agnieszka
Publicado: (2023)

Spinal tuberculosis: diagnosis and management
por: Rasouli, Mohammad, et al.
Publicado: (2012)

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene
por: Kanda, Kyoko, et al.
Publicado: (2009)

Restoration of Epithelial Sodium Channel Function by Synthetic Peptides in Pseudohypoaldosteronism Type 1B Mutants
por: Willam, Anita, et al.
Publicado: (2017)

A Novel SCNN1A Variation in a Patient with Autosomal-recessive Pseudohypoaldosteronism Type 1
por: Huneif, Mohammed Ayed, et al.
Publicado: (2022)

PReS-FINAL-2255: Primary pyomiositis in children: a challenging diagnosis
por: Moressa, V, et al.
Publicado: (2013)

Diagnosis and management of human borreliosis in Romania
por: Mihailescu, P, et al.
Publicado: (2014)

Pseudohypoaldosteronism in a Neonate Presenting as Life-Threatening Hyperkalemia
por: Attia, Najya A., et al.
Publicado: (2016)

SUN-184 Pseudohypoaldosteronism Presenting with Salt Wasting Crisis
por: Babar, Ghufran S
Publicado: (2020)

Secondary Pseudohypoaldosteronism Associated With Mild Hydronephrosis in a Newborn
por: Kodo, Kazuki, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_j3o8ql18l4bc7gh32gsfvn1a42