Intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome

Intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome

ग्रंथसूची विवरण
मुख्य लेखकों:	Woods, R, Ul-Haq, E, Wilkie, A, Jayamohan, J, Richards, P, Johnson, D, Lester, T, Wall, SA
स्वरूप:	Conference item
प्रकाशित:	2009

समान संसाधन

Reoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.
द्वारा: Woods, R, और अन्य
प्रकाशित: (2009)

Language development, hearing loss, and intracranial hypertension in children with TWIST1-confirmed Saethre-Chotzen syndrome
द्वारा: Kilcoyne, S, और अन्य
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Disruption of TWIST1 translation by 5′ UTR variants in Saethre‐Chotzen syndrome
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Síndrome de Saethre-Chotzen
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Case report: Primary stabbing headache treated with melatonin in Saethre-Chotzen syndrome
द्वारा: Florian Frank, और अन्य
प्रकाशित: (2023-10-01)

Correção de estrabismo em paciente com síndrome de Saethre-Chotzen
द्वारा: Thiago Gonçalves dos Santos Martins, और अन्य
प्रकाशित: (2013-06-01)

Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome
द्वारा: Camilla S Teng, और अन्य
प्रकाशित: (2018-10-01)

Prenatal diagnosis of chromothripsis causing complex chromosomal rearrangement involving chromosomes 5, 7 and 11 leading to TWIST1 deletion and Saethre-Chotzen syndrome
द्वारा: Ivana Joksic, और अन्य
प्रकाशित: (2025-01-01)

Case report: A third variant in the 5′ UTR of TWIST1 creates a novel upstream translation initiation site in a child with Saethre-Chotzen syndrome
द्वारा: Diaz-Gonzalez, F, और अन्य
प्रकाशित: (2023)

Case report: A third variant in the 5′ UTR of TWIST1 creates a novel upstream translation initiation site in a child with Saethre-Chotzen syndrome
द्वारा: Francisca Diaz-Gonzalez, और अन्य
प्रकाशित: (2023-01-01)

Pharmacological targeting of KDM6A and KDM6B, as a novel therapeutic strategy for treating craniosynostosis in Saethre-Chotzen syndrome
द्वारा: Clara Pribadi, और अन्य
प्रकाशित: (2020-12-01)

Raised intracranial pressure is frequent in untreated nonsyndromic unicoronal synostosis and does not correlate with severity of phenotypic features.
द्वारा: Eley, K, और अन्य
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The incidence of raised intracranial pressure in nonsyndromic sagittal craniosynostosis following primary surgery.
द्वारा: Thomas, G, और अन्य
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Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis.
द्वारा: Wilkie, A, और अन्य
प्रकाशित: (2010)

Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure.
द्वारा: Bendon, C, और अन्य
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Implications of a vertex bulge following modified strip craniectomy for sagittal synostosis.
द्वारा: Marucci, D, और अन्य
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Functional analysis of natural mutations in two TWIST protein motifs.
द्वारा: Funato, N, और अन्य
प्रकाशित: (2005)

Atypical Crouzon Syndrome With a Novel Cys62Arg Mutation in FGFR2 Presenting With Sagittal Synostosis.
द्वारा: Sharma, V, और अन्य
प्रकाशित: (2012)

Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure
द्वारा: Bendon Charlotte L, और अन्य
प्रकाशित: (2012-11-01)

Clinical Manifestations of Intracranial Hypertension and Herniation Syndrome
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Intracranial haemorrhage in Childhood ITP: An unfortunate twist of fate
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The Prevalence of Polycystic Ovary Syndrome in Women with Idiopathic Intracranial Hypertension
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A Case of Neurobrucellosis That Mimicks Increased Intracranial Hypertension Syndrome
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POEMS Syndrome with Transient Intracranial Hypertension and Nonspecific Gait Disturbance
द्वारा: Vivek Rauniyar, और अन्य
प्रकाशित: (2013-10-01)

Idiopathic intracranial hypertension.
द्वारा: Wakerley, B, और अन्य
प्रकाशित: (2014)

Idiopathic Intracranial Hypertension
द्वारा: J Gordon Millichap
प्रकाशित: (2001-08-01)

Idiopathic Intracranial Hypertension
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द्वारा: Lalitha Sivaswamy
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Idiopathic intracranial hypertension
द्वारा: G. Vandekerckhove, और अन्य
प्रकाशित: (2014-09-01)

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Cerebral venous etiology of intracranial hypertension and differentiation from idiopathic intracranial hypertension
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Intracranial venous manometry in patients with idiopathic intracranial hypertension
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FGFR3 P250R mutation increases the risk of reoperation in apparent 'nonsyndromic' coronal craniosynostosis.
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