Access to kidney transplantation for patients with end-stage renal failure in Maghreb countries: state of art and recommendations
In conclusion, access to transplantation remains low in the Maghreb countries. All the modalities (living donor with enlargement of the circle of donors, deceased donors) must be further developed. Recommendations were issued to support activity.PMID:38314548 | DOI:10.1684/ndt.2024.62 (Source: Nephrologie and Therapeutique)
Source: Nephrologie and Therapeutique - February 5, 2024 Category: Urology & Nephrology Authors: Macher Marie-Alice Bacha Mohamed Mongi Soualmia Amel Laouad Inass Sfar Imen Jacquelinet Christian Me çabih Fateh Younous Said Bayar Rached Ziadi Jalel Nebab Abed El Kader Barry Na ïma Nouvellon H élène Gozzerino Agathe Durin Laurent Ben Abdallah Taieb Source Type: research
Abortion in Melilla: barriers to ocean and frontier
CONCLUSIONS: The barriers to abortion access identified in this study represent a violation of women's reproductive rights in Melilla. Urgent action is required to review the current process, ensuring that access is improved and the right to safe abortion is guaranteed for all women residing in Melilla.PMID:38309253 | DOI:10.1016/j.gaceta.2024.102355 (Source: Gaceta Sanitaria)
Source: Gaceta Sanitaria - February 3, 2024 Category: International Medicine & Public Health Authors: Eva Est évanez Jiménez Maite Cruz Piqueras Source Type: research
Patterns of practice survey for cervical cancer brachytherapy in Morocco
This study surveyed radiation oncologists in Morocco to explore current practices and perspectives on brachytherapy for cervix cancer. (Source: Brachytherapy)
Source: Brachytherapy - February 3, 2024 Category: Cancer & Oncology Authors: Tarik Chekrine, Fatima Zahra Bellefkih, Ghita Hatim, Zineb Bouchbika, Nadia Benchakroun, Hassan Jouhadi, Nezha Tawfiq, Souha Sahraoui Tags: Original Article Source Type: research
Hepatic focal lesions and constitutional syndrome, is it always cancer?
We present the case of a 51-year-old male from Morocco diagnosed with hepatic SOLs in the context of abdominal pain and constitutional syndrome.PMID:38305672 | DOI:10.17235/reed.2024.10195/2023 (Source: Revista Espanola de Enfermedades Digestivas)
Source: Revista Espanola de Enfermedades Digestivas - February 2, 2024 Category: Gastroenterology Authors: Eugenia Navarro Moreno Samia Hallouch Toutouh Sebasti án Pinotchet Marta Casado Mart ín Jos é Luis Vega Sáenz Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
Management of Acute Complications of Sickle Cell Disease
Pediatr Ann. 2024 Feb;53(2):e47-e51. doi: 10.3928/19382359-20231205-03. Epub 2024 Feb 1.ABSTRACTSickle cell disease (SCD) is a group of inherited autosomal recessive disorders that affect hemoglobin structure. The presence of this mutated form of hemoglobin, hemoglobin S, results in the abnormally ("sickle") shaped cells. These sickle-shaped red blood cells lead to the disruption of blood flow in small vessels and result in a myriad of complications. Pain, excruciating and unpredictable, is the hallmark of the disease. In addition, many organs are affected, including but not limited to brain, kidneys, bones, and lungs. Thi...
Source: Pediatric Annals - February 1, 2024 Category: Pediatrics Authors: Sabina Shamayeva Perry Morocco Source Type: research
