Cargando…

Silver: Russell Syndrome with Cryptorchidism

Detalles Bibliográficos
Autores principales:	Reddy, H Babul, Neelaveni, K, Kumar, KVS Hari
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2013
Materias:	Letters to Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853611/ https://www.ncbi.nlm.nih.gov/pubmed/24349852 http://dx.doi.org/10.4103/2141-9248.121226

Ejemplares similares

Cornelia de Lange syndrome
por: Reddy, H. Babul, et al.
Publicado: (2013)

Clinical spectrum of Silver - Russell syndrome
por: Varma, Sapna N.K., et al.
Publicado: (2013)

Russell's sign in obsessive–compulsive disorder
por: Rikhari, Praveen, et al.
Publicado: (2021)

Silver-Russell Syndrome: A Case Report
por: Kumar, Sunil, et al.
Publicado: (2008)

Epigenotype–phenotype correlations in Silver–Russell syndrome
por: Wakeling, E L, et al.
Publicado: (2010)

Tuft of Hair at an Unusual Location
por: Hari Kumar, KVS, et al.
Publicado: (2013)

A patient with Temple syndrome satisfying the clinical diagnostic criteria of Silver–Russell syndrome
por: Goto, Masahide, et al.
Publicado: (2016)

The Incidence of Neonatal Cryptorchidism in Sfax, Tunisia
por: HAYET, Zitouni, et al.
Publicado: (2015)

An interesting case of Rathke's cleft cyst presenting as bilateral cryptorchidism
por: Hanmayyagari, Babul Reddy, et al.
Publicado: (2013)

Mighty journals, mega trials, and modest points
por: Kumar, K.V.S. Hari, et al.
Publicado: (2016)

Bilateral gynecomastia: A rare presentation of thyrotoxicosis
por: Kumar, K.V.S. Hari, et al.
Publicado: (2013)

Acrocyanosis with intrahepatic carcinoid tumor
por: Hari Kumar, K.V.S., et al.
Publicado: (2014)

Massive multinodular goiter with stridor
por: Kumar, K.V.S. Hari, et al.
Publicado: (2012)

Russell–Silver syndrome associated with low conus medullaris
por: Gabor, Larisa, et al.
Publicado: (2016)

An Unusual Association: Silver-Russell Syndrome and Ectopic Thyroid
por: Lahmamssi, Fatima-Zahra, et al.
Publicado: (2022)

Executive functioning in adolescents and adults with Silver-Russell syndrome
por: Burgevin, Mélissa, et al.
Publicado: (2023)

Benefits of orchidopexy on the fertility of adult men with bilateral cryptorchidism
por: Zhang, Yan, et al.
Publicado: (2018)

Genetic diagnosis of Beckwith Wiedemann syndrome and Silver-Russell syndrome
por: Kim, Yoo-Mi, et al.
Publicado: (2013)

A rare gastric lesion: Russel body gastritis
por: Yalçın, Mehmet Suat, et al.
Publicado: (2020)

Silver-Russell syndrome: genetic basis and molecular genetic testing
por: Eggermann, Thomas, et al.
Publicado: (2010)

Orthodontic Management of Silver-Russell Syndrome. A Case Report
por: Ioannidou-Marathiotou, Ioulia, et al.
Publicado: (2012)

Clinical characteristics and imprinting analysis of Chinese Silver Russell Syndrome
por: Wu, Di, et al.
Publicado: (2015)

Uncovering common pathogenic transcriptional dysregulations in Silver-Russell syndrome
por: Bohne, Florian, et al.
Publicado: (2014)

Phenotype of genetically confirmed Silver-Russell syndrome beyond childhood
por: Lokulo-Sodipe, Oluwakemi, et al.
Publicado: (2020)

Parthenogenetic chimaerism/mosaicism with a Silver-Russell syndrome-like phenotype
por: Yamazawa, K, et al.
Publicado: (2010)

Silver–Russell syndrome in a patient with somatic mosaicism for upd(11)mat identified by buccal cell analysis
por: Luk, Ho‐Ming, et al.
Publicado: (2016)

A rare case of Silver–Russell syndrome associated with growth hormone deficiency and urogenital abnormalities
por: Prasad, Namburi Rajendra, et al.
Publicado: (2012)

Molecular and Clinical Studies in 138 Japanese Patients with Silver-Russell Syndrome
por: Fuke, Tomoko, et al.
Publicado: (2013)

The clinical and molecular genetic study of 20 Silver Russell Syndrome cases
por: Gong, Chunxiu, et al.
Publicado: (2013)

Seminoma in a Man with Russell-Silver Syndrome Presenting with Testicular Torsion
por: Funada, Satoshi, et al.
Publicado: (2016)

Correction of the axial and appendicular deformities in a patient with Silver-Russel syndrome
por: Al Kaissi, Ali, et al.
Publicado: (2015)

Behavioural abnormalities in a novel mouse model for Silver Russell Syndrome
por: McNamara, Grainne Iseult, et al.
Publicado: (2016)

Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes
por: Mackay, Deborah J.G., et al.
Publicado: (2019)

Clinical Application of Sequential Epigenetic Analysis for Diagnosis of Silver–Russell Syndrome
por: Kim, Soo Yeon, et al.
Publicado: (2021)

Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver–Russell Syndrome
por: Lin, Hsiang-Yu, et al.
Publicado: (2021)

Chronic Hypercapnic Respiratory Failure in an Adult Patient with Silver-Russell Syndrome
por: Hakamata, Mariko, et al.
Publicado: (2021)

Maternal UPD of chromosome 7 in a patient with Silver‐Russell syndrome and Pendred syndrome
por: Zhang, Chuan, et al.
Publicado: (2020)

Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndrome
por: Chang, Suhee, et al.
Publicado: (2020)

ODP373 A Tale of Two Syndromes: Coexistence of Russell-Silver and Klinefelter Syndrome
por: Pillai, Chanthu
Publicado: (2022)

Russell Silver syndrome: a perspective on growth and the influence of growth hormone therapy
por: Mascarenhas, J. V., et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_j0b3es6jk5du3ri0ctsrt24g56