Search Results - "Baas, Martijn"

Preaxial polydactyly of the foot: Clinical and genetic implications for the orthopedic practice based on a literature review and 76 patients by Burger, Elise B, Baas, Martijn, Hovius, Steven E R, Hoogeboom, A Jeannette M, van Nieuwenhoven, Christianne A

“…Background and purpose - Preaxial polydactyly of the foot is a rare malformation and clinicians are often unfamiliar with the associated malformations and…”
Get full text

A systematic review on the sensory reinnervation of free flaps for tongue reconstruction: Does improved sensibility imply functional benefits? by Baas, Martijn, Duraku, Liron S, Corten, Eveline M.L, Mureau, Marc A.M

“…Summary Background Tongue reconstruction after (hemi)glossectomy including sensory recovery is challenging. Although sensory recovery could improve functional…”
Get full text

Arthroscopic versus open distal hemi-trapeziectomy without interposition in CMC thumb joint osteoarthritis 2-year results of a randomized controlled trial by van Laarhoven, Cecile M.C.A., Baas, Martijn, Qi, Hongchao, Coert, J.Henk, Zuidam, J. Michiel, Koch, A. Richard

Get full text

Arthroscopic versus Open Distal Hemitrapeziectomy without Interposition: 2-Year Results of a Randomized Controlled Trial by van Laarhoven, Cecile M. C. A., Baas, Martijn, Qi, Hongchao, Coert, J. Henk, Zuidam, J. Michiel, Koch, A. Richard

“…Distal hemitrapeziectomy is suggested as an alternative for total trapeziectomy for carpometacarpal thumb joint osteoarthritis, when the…”
Get full text

Variant type and position predict two distinct limb phenotypes in patients with GLI3-mediated polydactyly syndromes by Baas, Martijn, Burger, Elise Bette, van den Ouweland, Ans Mw, Hovius, Steven Er, de Klein, Annelies, van Nieuwenhoven, Christianne A, Galjaard, Robert Jan H

“…Pathogenic DNA variants in the GLI-Kruppel family member 3 ( gene are known to cause multiple syndromes: for example, Greig syndrome, preaxial polydactyly-type…”
Get more information

Documenting Combined Congenital Upper Limb Anomalies Using the Oberg, Manske, and Tonkin Classification: Implications for Epidemiological Research and Outcome Comparisons by Baas, Martijn, Zwanenburg, Pieter R., Hovius, Steven E.R., van Nieuwenhoven, Christianne A.

“…Congenital upper limb anomalies (CULAs) exhibit a wide spectrum of phenotypic manifestations. To help the clinician evaluating this variety of CULAs, the…”
Get full text

Motor nerve transfers for reconstruction of traumatic upper extremity nerve injuries – a scoping review by Duraku, Liron S., Chaudhry, Tahseen, George, Samuel, Madura, Tomas, Zuidam, J. Michiel, Hundepool, Caroline A., Teunis, Teun, Baas, Martijn, Ramadan, Sami, Burahee, Abdus S., Power, Dominic M.

Get full text

Controversies in Poland Syndrome: Alternative Diagnoses in Patients With Congenital Pectoral Muscle Deficiency by Baas, Martijn, Burger, Elise B., Sneiders, Dimitri, Galjaard, Robert-Jan H., Hovius, Steven E.R., van Nieuwenhoven, Christianne A.

“…Poland syndrome was first described as a deficiency of the pectoral muscle with ipsilateral symbrachydactyly. Currently, numerous case reports describe…”
Get full text

A point mutation in the pre-ZRS disrupts sonic hedgehog expression in the limb bud and results in triphalangeal thumb–polysyndactyly syndrome by Potuijt, Jacob W P, Baas, Martijn, Sukenik-Halevy, Rivka, Douben, Hannie, Nguyen, Picard, Venter, Deon J, Gallagher, Renée, Swagemakers, Sigrid M, Hovius, Steven E R, van Nieuwenhoven, Christianne A, Galjaard, Robert-Jan H, van der Spek, Peter J, Ahituv, Nadav, de Klein, Annelies

“…Purpose The zone of polarizing activity regulatory sequence (ZRS) is an enhancer that regulates sonic hedgehog during embryonic limb development. Recently,…”
Get full text

Re-innervation patterns by peptidergic Substance-P, non-peptidergic P2X3, and myelinated NF-200 nerve fibers in epidermis and dermis of rats with neuropathic pain by Duraku, Liron S., Hossaini, Mehdi, Schüttenhelm, Barthold N., Holstege, Joan C., Baas, Martijn, Ruigrok, Tom J.H., Walbeehm, Erik T.

“…Nerve endings in the epidermis, termed nociceptors, conduct information on noxious stimuli to the central nervous system. The precise role of epidermal nerve…”
Get full text

Identification of Associated Genes and Diseases in Patients With Congenital Upper-Limb Anomalies: A Novel Application of the OMT Classification by Baas, Martijn, Stubbs, Andrew P., van Zessen, David B., Galjaard, Robert-Jan H., van der Spek, Peter J., Hovius, Steven E.R., van Nieuwenhoven, Christianne A.

“…Congenital upper-limb anomalies (CULA) can present as a part of a syndrome or association. There is a wide spectrum of CULA, each of which might be related to…”
Get full text

Long-term follow-up of peptidergic and nonpeptidergic reinnervation of the epidermis following sciatic nerve reconstruction in rats by Kambiz, Shoista, Duraku, Liron S, Baas, Martijn, Nijhuis, Tim H J, Cosgun, Saniye G, Hovius, Steven E R, Ruigrok, Tom J H, Walbeehm, Erik T

“…Peripheral nerve injuries are a commonly encountered clinical problem and often result in long-term functional deficits. The current gold standard for…”
Get full text

Intrafamilial variability of the triphalangeal thumb phenotype in a Dutch population: Evidence for phenotypic progression over generations? by Baas, Martijn, Potuijt, Jacob W.P., Hovius, Steven E.R., Hoogeboom, A. Jeannette M., Galjaard, Robert‐Jan H., van Nieuwenhoven, Christianne A.

“…Triphalangeal thumbs (TPTs) are regularly caused by mutations in the ZRS in LMBR1. Phenotypic variability can be present in TPT‐families. However, recent…”
Get full text

Letter to the editor regarding: “Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial polydactyly patients” Clinica Chimica acta 433 (2014) 195–199 by Baas, Martijn, Galjaard, Robert-Jan, der Spek, Peter van, Hovius, Steven E.R., van Nieuwenhoven, Christianne A.

Get full text

Preaxial polydactyly of the foot by Burger, Elise B, Baas, Martijn, Hovius, Steven E R, Hoogeboom, A Jeannette M, van Nieuwenhoven, Christianne A

“…Background and purpose - Preaxial polydactyly of the foot is a rare malformation and clinicians are often unfamiliar with the associated malformations and…”
Get full text