Cargando…

McLeod Syndrome: Report of an Indian family with phenotypic heterogeneity

Mostrar otras versiones (1)

Detalles Bibliográficos
Autores principales:	Chakravarty, A., Bhattacharya, P., Banerjee, D., Mukherjee, S.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications 2011
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141489/ https://www.ncbi.nlm.nih.gov/pubmed/21808490 http://dx.doi.org/10.4103/0972-2327.82827

Ejemplares similares

McLeod syndrome and acanthocytosis
por: Mehndiratta, M.
Publicado: (2011)

Mcleod syndrome: Report of an Indian family with phenotypic heterogeneity
por: Chakravarty, Ambar, et al.
Publicado: (2011)

Brigade-Surgeon McLeod
Publicado: (1892)

Endosomal recycling defects link Huntington’s disease with McLeod syndrome
por: Marsan, Elise, et al.
Publicado: (2022)

Chronic granulomatous disease, the McLeod phenotype and the contiguous gene deletion syndrome-a review
por: Watkins, Casey E, et al.
Publicado: (2011)

McLeod syndrome with a novel XK frameshift mutation: A case report
por: Xia, Shilin, et al.
Publicado: (2022)

A Case of McLeod’s Syndrome Presenting with Severe Decompensated Heart Failure
por: Boppana, Hemanth K., et al.
Publicado: (2023)

A patient with McLeod syndrome showing involvement of the central sensorimotor tracts for the legs
por: Murakami, Takenobu, et al.
Publicado: (2019)

Advances in time series methods and applications: the A. Ian McLeod festschrift
por: Li, Wai, et al.
Publicado: (2016)

Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein
por: Urata, Yuka, et al.
Publicado: (2019)

XK is a partner for VPS13A: a molecular link between Chorea-Acanthocytosis and McLeod Syndrome
por: Park, Jae-Sook, et al.
Publicado: (2020)

A case of McLeod syndrome caused by a nonsense variation c.942G>A in the XK gene: A case report
por: Ying, Yanling, et al.
Publicado: (2023)

Case II.—Compound Comminuted Fracture of Leg: Tetanus: Amputation: Death. Under the Care of Dr. K. McLeod
Publicado: (1874)

Chronic granulomatous disease and McLeod syndrome: Stem cell transplant and transfusion support in a 2-year-old patient—a case report
por: Helander, Louise, et al.
Publicado: (2022)

Case I.—Compound Dislocation of Ankle Joint and Compound Fracture of Tarsus: Excision: Recovery. Under the Care of Dr. K. McLeod
por: Ghose, Jogendro Nath
Publicado: (1874)

Novel single base-pair deletion in exon 1 of XK gene leading to McLeod syndrome with chorea, muscle wasting, peripheral neuropathy, acanthocytosis and haemolysis
por: Wiethoff, Sarah, et al.
Publicado: (2014)

Case III.—Scrotal Elephantiasis and Hæmatocele: Tapping: Inflammation and Sloughing of Scrotum: Removal of Elephantoid Mass: Tetanus: Death. Under the Care of Dr. K. McLeod
Publicado: (1874)

Colonel Kenneth MacLeod
Publicado: (1923)

Swyer-James-MacLeod syndrome in pregnancy: A case report
por: Al-Bakri, Omar, et al.
Publicado: (2022)

Adult diagnosis of Swyer-James-MacLeod syndrome: a case report
por: Capela, Carlos, et al.
Publicado: (2011)

Lieutenant George Munro MacLeod
Publicado: (1915)

Mr. M'Leod, on the Bulam Fever
por: M'Leod, John
Publicado: (1816)

Dr. Norman K. MacLeod
Publicado: (1913)

Swyer–James–MacLeod syndrome with an anomalous origin of coronary artery: Case report
por: Aşker, Selvi, et al.
Publicado: (2013)

Swyer-James-MacLeod syndrome with unilateral pulmonary fibrosis: a case report
por: Abdulla, Omar, et al.
Publicado: (2017)

Mazabraud syndrome associated with McCune-Albright syndrome
por: Biazzo, Alessio, et al.
Publicado: (2017)

Graham Ross MacLeod (facing camera)
por: CERN PhotoLab
Publicado: (1964)

Dr K. M'Leod on Cure of Hernia
Publicado: (1883)

COVID-19-associated pneumonia in Swyer-James-MacLeod syndrome: A case report
por: Bitsani, Aikaterini, et al.
Publicado: (2022)

Multimodal imaging findings in an adult case of Swyer‐James‐MacLeod syndrome
por: Kawasuji, Hitoshi, et al.
Publicado: (2017)

VATS bullectomy and apical pleurectomy for spontaneous pneumothorax in a young patient with Swyer-James-Mc Leod syndrome: case report presentation and literature review focusing on surgically treated cases
por: Panagopoulos, Nikolaos, et al.
Publicado: (2014)

Semi-invasive aspergillosis in an immunocompetent patient with Swyer-James-MacLeod Syndrome: a case report
por: Salgado, Sara MST, et al.
Publicado: (2010)

Swyer-James-MacLeod syndrome presenting as spontaneous pneumothorax in an adult: Case report and review of literature
por: Conti, Luigi, et al.
Publicado: (2021)

Broad Phenotypic Heterogeneity and Multisystem Involvement in Single mtDNA Deletion-associated Pearson Syndrome
por: Finsterer, Josef, et al.
Publicado: (2018)

A Suspected Case and Literature Review of McCune-Albright Syndrome
por: Jung, Kyung Eun, et al.
Publicado: (2014)

Psychosocial and emotional impact of strabismus on Indian families
por: Gogate, Parikshit
Publicado: (2010)

Regional ventilation/perfusion mismatch pattern in patient with Swyer James (MacLeod's) syndrome
por: Sager, Sait, et al.
Publicado: (2014)

NDUFAF5 variants manifest phenotypically heterogeneously
por: Finsterer, Josef
Publicado: (2018)

Phenotypic Heterogeneity of the m.14459G>A Mutation
por: Finsterer, Josef, et al.
Publicado: (2017)

A proof-of-concept study of growth hormone in children with Phelan–McDermid syndrome
por: Sethuram, S., et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_ibmo5cti9ns9utt73gei3h1jut