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Results for
""Craniosynostoses""[mesh_terms]

31 Results

Searching titles within these results

Craniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure.

Esmee Oussoren, Irene M J Mathijssen, Margreet Wagenmakers, Rob M Verdijk, Hansje H Bredero-Boelhouwer, Marie-Lise C van Veelen-Vincent, Jan C van der Meijden, Johanna M P van den Hout, George J G Ruijter, Ans T van der Ploeg, Mirjam Langeveld

Journal of inherited metabolic disease 2019;41(6):1247-1258

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Bohring-Opitz (Oberklaid-Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis.

Rob Hastings, Jan-Maarten Cobben, Gabriele Gillessen-Kaesbach, Judith Goodship, Hanne Hove, Susanne Kjaergaard, Helena Kemp, Helen Kingston, Peter Lunt, Sahar Mansour, Ruth McGowan, Kay Metcalfe, Catherine Murdoch-Davis, Mary Ray, Marlène Rio, Sarah Smithson, John Tolmie, Peter Turnpenny, Bregje van Bon, Dagmar Wieczorek, Ruth Newbury-Ecob

European journal of human genetics : EJHG 2011;19(5):513-9

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Craniosynostosis and metabolic bone disorder. A review.

F Di Rocco, A Rothenbuhler, V Cormier Daire, J Bacchetta, C Adamsbaum, G Baujat, M Rossi, A Lingart

Neuro-Chirurgie 2020;65(5):258-263

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Syndromic Synostosis: Frontofacial Surgery.

Kevin Chen, Katelyn Kondra, Eric Nagengast, Jeffrey A Hammoudeh, Mark M Urata

Oral and maxillofacial surgery clinics of North America 2022;34(3):459-466

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A multi-omic brain gut microbiome signature differs between IBS subjects with different bowel habits.

Rachel P Sarnoff, Ravi R Bhatt, Vadim Osadchiy, Tien Dong, Jennifer S Labus, Lisa A Kilpatrick, Zixi Chen, Vishvak Subramanyam, Yurui Zhang, Benjamin M Ellingson, Bruce Naliboff, Lin Chang, Emeran A Mayer, Arpana Gupta

Neuropharmacology 2023;225():109381

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Association of novel mutation in TRPV4 with familial nonsyndromic craniosynostosis with complete penetrance and variable expressivity.

Tenzin Gayden, Gabriel Crevier-Sorbo, Wajih Jawhar, Christine Saint-Martin, Robert Eveleigh, Mirko S Gilardino, Natascia Anastasio, Yannis Trakadis, Angelia V Bassenden, Albert M Berghuis, Nada Jabado, Roy W R Dudley

Journal of neurosurgery. Pediatrics 2023;31(6):584-592

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Shprintzen - Goldberg syndrome without intellectual disability: A clinical report and review of literature.

Elisa Docampo, Camille Chatelain, Léna Kukor, Sophie Bailleux, Vincent Bours, Saskia Bulk

European journal of medical genetics 2025;73():104985

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Intracranial Volume Post Cranial Expansion Surgery Using Three-Dimensional Computed Tomography Scan Imaging in Children With Craniosynostosis.

Shukriyah Sulong, Azmi Alias, Fadzlishah Johanabas, Johari Yap Abdullah, Badrisyah Idris

The Journal of craniofacial surgery 2020;31(1):46-50

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Reducing glucose infusion safely prevents hyperglycemia in post-surgical children.

Sascha C A T Verbruggen, Carlijn T I de Betue, Henk Schierbeek, Shaji Chacko, Leon N A van Adrichem, Jennifer Verhoeven, Johannes B van Goudoever, Koen F M Joosten

Clinical nutrition (Edinburgh, Scotland) 2012;30(6):786-92

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Novel compound heterozygous WDR35 variants in a Chinese patient associated with cranioectodermal dysplasia and ectopic testis: a case report and review of the literature.

Lijie Li, Cuihua Liu, Ming Tian, Guangbo Li, Jitong Li

BMC pediatrics 2023;23(1):407

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Craniosynostosis, delayed closure of the fontanelle, anal, genitourinary, and skin abnormalities (CDAGS syndrome): first report in a Mexican patient and review of the literature.

Rodrigo Pastrana-Ayala, Gretty L Peña-Castro, Adriana M Valencia-Herrera, Carlos A Mena-Cedillos, Sonia Toussaint-Caire, Yumiko I Akaki-Carreño, Constanza García-Delgado, Veronica F Morán-Barroso, Mirna Toledo-Bahena

International journal of dermatology 2017;56(4):435-439

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Cerebral salt wasting syndrome after calvarial remodeling in craniosynostosis.

Jun-Hee Byeon, Gyeol Yoo

Journal of Korean medical science 2006;20(5):866-9

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Unclassifiable craniosynostosis phenotypes, FGFR2 Trp290 mutations, acanthosis nigricans, and unpaired cysteine mutations.

M Michael Cohen

American journal of medical genetics 2003;113(1):1-3

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The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.

Z Vajo, C A Francomano, D J Wilkin

Endocrine reviews 2000;21(1):23-39

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Hyponatremia in the neurosurgical patient: diagnosis and management.

Chad D Cole, Oren N Gottfried, James K Liu, William T Couldwell

Neurosurgical focus 2004;16(4):E9

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Results: 1 – 15 / 31

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Results for ""Craniosynostoses""[mesh_terms]

Craniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure.

Bohring-Opitz (Oberklaid-Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis.

Craniosynostosis and metabolic bone disorder. A review.

Syndromic Synostosis: Frontofacial Surgery.

A multi-omic brain gut microbiome signature differs between IBS subjects with different bowel habits.

Association of novel mutation in TRPV4 with familial nonsyndromic craniosynostosis with complete penetrance and variable expressivity.

Shprintzen - Goldberg syndrome without intellectual disability: A clinical report and review of literature.

Intracranial Volume Post Cranial Expansion Surgery Using Three-Dimensional Computed Tomography Scan Imaging in Children With Craniosynostosis.

Reducing glucose infusion safely prevents hyperglycemia in post-surgical children.

Novel compound heterozygous WDR35 variants in a Chinese patient associated with cranioectodermal dysplasia and ectopic testis: a case report and review of the literature.

Craniosynostosis, delayed closure of the fontanelle, anal, genitourinary, and skin abnormalities (CDAGS syndrome): first report in a Mexican patient and review of the literature.

Cerebral salt wasting syndrome after calvarial remodeling in craniosynostosis.

Unclassifiable craniosynostosis phenotypes, FGFR2 Trp290 mutations, acanthosis nigricans, and unpaired cysteine mutations.

The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.

Hyponatremia in the neurosurgical patient: diagnosis and management.

Results for
""Craniosynostoses""[mesh_terms]