Is open anterior advantageous to posterior decompression and reconstruction in fresh A < sub > 3 < /sub > to C < sub > 3 < /sub > /AO type thoracolumbar junction fractures? A systematic review
CONCLUSIONS: The anterior approach is demanding and is associated with a higher rate of surgical complications compared to the posterior approach. The limitations of the selected studies included inconsistence in the: 1) approaches selection, 2) classifications of the fracture types and the neurological status and 3) variety of instrumentations used.PROSPERO ID: CRD42023484222.PMID:38590235 | DOI:10.1080/17434440.2024.2341109 (Source: Expert Review of Medical Devices)
Source: Expert Review of Medical Devices - April 9, 2024 Category: Medical Devices Authors: P Korovessis Vasileios Syrimpeis Alkis Korovesis Source Type: research
Recent advances in toxicological research of di-(2-ethylhexyl)-phthalate: Focus on endoplasmic reticulum stress pathway
This study offers possible targets and approaches for addressing various DEHP-induced toxicity.PMID:38593956 | DOI:10.1016/j.chemosphere.2024.141922 (Source: Chemosphere)
Source: Chemosphere - April 9, 2024 Category: Chemistry Authors: Jiten Singh Ashok Jangra Dinesh Kumar Source Type: research
Recent advances in toxicological research of di-(2-ethylhexyl)-phthalate: Focus on endoplasmic reticulum stress pathway
This study offers possible targets and approaches for addressing various DEHP-induced toxicity.PMID:38593956 | DOI:10.1016/j.chemosphere.2024.141922 (Source: Chemosphere)
Source: Chemosphere - April 9, 2024 Category: Chemistry Authors: Jiten Singh Ashok Jangra Dinesh Kumar Source Type: research
Is open anterior advantageous to posterior decompression and reconstruction in fresh A < sub > 3 < /sub > to C < sub > 3 < /sub > /AO type thoracolumbar junction fractures? A systematic review
CONCLUSIONS: The anterior approach is demanding and is associated with a higher rate of surgical complications compared to the posterior approach. The limitations of the selected studies included inconsistence in the: 1) approaches selection, 2) classifications of the fracture types and the neurological status and 3) variety of instrumentations used.PROSPERO ID: CRD42023484222.PMID:38590235 | DOI:10.1080/17434440.2024.2341109 (Source: Expert Review of Medical Devices)
Source: Expert Review of Medical Devices - April 9, 2024 Category: Medical Devices Authors: P Korovessis Vasileios Syrimpeis Alkis Korovesis Source Type: research
Recent advances in toxicological research of di-(2-ethylhexyl)-phthalate: Focus on endoplasmic reticulum stress pathway
This study offers possible targets and approaches for addressing various DEHP-induced toxicity.PMID:38593956 | DOI:10.1016/j.chemosphere.2024.141922 (Source: Chemosphere)
Source: Chemosphere - April 9, 2024 Category: Chemistry Authors: Jiten Singh Dinesh Kumar Ashok Jangra Source Type: research
Recent advances in toxicological research of di-(2-ethylhexyl)-phthalate: Focus on endoplasmic reticulum stress pathway
This study offers possible targets and approaches for addressing various DEHP-induced toxicity.PMID:38593956 | DOI:10.1016/j.chemosphere.2024.141922 (Source: Chemosphere)
Source: Chemosphere - April 9, 2024 Category: Chemistry Authors: Jiten Singh Dinesh Kumar Ashok Jangra Source Type: research
Is read-across for chemicals comparable to medical device equivalence and where to use it for conformity assessment?
Regul Toxicol Pharmacol. 2024 Apr 6:105622. doi: 10.1016/j.yrtph.2024.105622. Online ahead of print.ABSTRACTNovel medical devices must conform to medical device regulation (MDR) for European market entry. Likewise, chemicals must comply with the Registration, Evaluation, Authorization and Restriction of Chemicals (REACh) regulation. Both pose regulatory challenges for manufacturers, but concordantly provide an approach for transferring data from an already registered device or compound to the one undergoing accreditation. This is called equivalence for medical devices and read-across for chemicals. Although read-across is ...
Source: Regulatory Toxicology and Pharmacology : RTP - April 8, 2024 Category: Toxicology Authors: Jan S ündermann Annette Bitsch Rupert Kellner Theodor Doll Source Type: research
Is read-across for chemicals comparable to medical device equivalence and where to use it for conformity assessment?
Regul Toxicol Pharmacol. 2024 Apr 6:105622. doi: 10.1016/j.yrtph.2024.105622. Online ahead of print.ABSTRACTNovel medical devices must conform to medical device regulation (MDR) for European market entry. Likewise, chemicals must comply with the Registration, Evaluation, Authorization and Restriction of Chemicals (REACh) regulation. Both pose regulatory challenges for manufacturers, but concordantly provide an approach for transferring data from an already registered device or compound to the one undergoing accreditation. This is called equivalence for medical devices and read-across for chemicals. Although read-across is ...
Source: Regulatory Toxicology and Pharmacology : RTP - April 8, 2024 Category: Toxicology Authors: Jan S ündermann Annette Bitsch Rupert Kellner Theodor Doll Source Type: research
Is read-across for chemicals comparable to medical device equivalence and where to use it for conformity assessment?
Regul Toxicol Pharmacol. 2024 Apr 6:105622. doi: 10.1016/j.yrtph.2024.105622. Online ahead of print.ABSTRACTNovel medical devices must conform to medical device regulation (MDR) for European market entry. Likewise, chemicals must comply with the Registration, Evaluation, Authorization and Restriction of Chemicals (REACh) regulation. Both pose regulatory challenges for manufacturers, but concordantly provide an approach for transferring data from an already registered device or compound to the one undergoing accreditation. This is called equivalence for medical devices and read-across for chemicals. Although read-across is ...
Source: Regulatory Toxicology and Pharmacology : RTP - April 8, 2024 Category: Toxicology Authors: Jan S ündermann Annette Bitsch Rupert Kellner Theodor Doll Source Type: research
Is read-across for chemicals comparable to medical device equivalence and where to use it for conformity assessment?
Regul Toxicol Pharmacol. 2024 Apr 6:105622. doi: 10.1016/j.yrtph.2024.105622. Online ahead of print.ABSTRACTNovel medical devices must conform to medical device regulation (MDR) for European market entry. Likewise, chemicals must comply with the Registration, Evaluation, Authorization and Restriction of Chemicals (REACh) regulation. Both pose regulatory challenges for manufacturers, but concordantly provide an approach for transferring data from an already registered device or compound to the one undergoing accreditation. This is called equivalence for medical devices and read-across for chemicals. Although read-across is ...
Source: Regulatory Toxicology and Pharmacology : RTP - April 8, 2024 Category: Toxicology Authors: Jan S ündermann Annette Bitsch Rupert Kellner Theodor Doll Source Type: research
