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Showing 1 to 12 of 5409 entries
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Severe phenotype of X-linked dominant chondrodysplasia punctata.

Clinical case reports

Damseh N, Chong K, Marshall C, Kratz L, Teitelbaum R, Shannon P, Kannu P.
PMID: 28878897
Clin Case Rep. 2017 Jul 20;5(9):1435-1437. doi: 10.1002/ccr3.1008. eCollection 2017 Sep.

A prenatally ascertained case representing the more severe end of the X-linked dominant chondrodysplasia punctata (CDPX2).

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Damseh N, Chong K, Marshall C, et al. Severe phenotype of X-linked dominant chondrodysplasia punctata. Clin Case Rep. 2017;5(9):1435-1437doi: 10.1002/ccr3.1008.
Damseh, N., Chong, K., Marshall, C., Kratz, L., Teitelbaum, R., Shannon, P., & Kannu, P. (2017). Severe phenotype of X-linked dominant chondrodysplasia punctata. Clinical case reports, 5(9), 1435-1437. https://doi.org/10.1002/ccr3.1008
Damseh, Nadirah, et al. "Severe phenotype of X-linked dominant chondrodysplasia punctata." Clinical case reports vol. 5,9 (2017): 1435-1437. doi: https://doi.org/10.1002/ccr3.1008
Damseh N, Chong K, Marshall C, Kratz L, Teitelbaum R, Shannon P, Kannu P. Severe phenotype of X-linked dominant chondrodysplasia punctata. Clin Case Rep. 2017 Jul 20;5(9):1435-1437. doi: 10.1002/ccr3.1008. eCollection 2017 Sep. PMID: 28878897; PMCID: PMC5582310.
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Intravascular large B-cell lymphoma presenting as Richter's syndrome with cerebral involvement in a patient with chronic lymphocytic leukemia.

Clinical case reports

Puckrin R, Pop P, Ghorab Z, Keith J, Chodirker L, Lin Y, Callum J.
PMID: 28878900
Clin Case Rep. 2017 Jul 20;5(9):1444-1449. doi: 10.1002/ccr3.1087. eCollection 2017 Sep.

Intravascular large B-cell lymphoma (IVLBCL) is an aggressive non-Hodgkin's lymphoma which can present with B symptoms, rash, and neurological deterioration. Up to 10% of cases of IVLBCL are associated with other hematological neoplasms, including this extremely rare presentation of...

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Puckrin R, Pop P, Ghorab Z, et al. Intravascular large B-cell lymphoma presenting as Richter's syndrome with cerebral involvement in a patient with chronic lymphocytic leukemia. Clin Case Rep. 2017;5(9):1444-1449doi: 10.1002/ccr3.1087.
Puckrin, R., Pop, P., Ghorab, Z., Keith, J., Chodirker, L., Lin, Y., & Callum, J. (2017). Intravascular large B-cell lymphoma presenting as Richter's syndrome with cerebral involvement in a patient with chronic lymphocytic leukemia. Clinical case reports, 5(9), 1444-1449. https://doi.org/10.1002/ccr3.1087
Puckrin, Robert, et al. "Intravascular large B-cell lymphoma presenting as Richter's syndrome with cerebral involvement in a patient with chronic lymphocytic leukemia." Clinical case reports vol. 5,9 (2017): 1444-1449. doi: https://doi.org/10.1002/ccr3.1087
Puckrin R, Pop P, Ghorab Z, Keith J, Chodirker L, Lin Y, Callum J. Intravascular large B-cell lymphoma presenting as Richter's syndrome with cerebral involvement in a patient with chronic lymphocytic leukemia. Clin Case Rep. 2017 Jul 20;5(9):1444-1449. doi: 10.1002/ccr3.1087. eCollection 2017 Sep. PMID: 28878900; PMCID: PMC5582220.
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Breast reconstruction in pregnancy: a case report of multidisciplinary team approach in immediate autologous flap reconstruction for pregnancy-associated breast cancer.

Clinical case reports

Chirappapha P, Thaweepworadej P, Ngamphaiboon N, Sukprasert M, Sukarayothin T, Leesombatpaiboon M.
PMID: 28878901
Clin Case Rep. 2017 Jul 20;5(9):1450-1453. doi: 10.1002/ccr3.1092. eCollection 2017 Sep.

This report presents the results of immediate breast reconstruction with autologous flap in Pregnancy-associated breast cancer (PABC). There was no obstetrics and surgical complications in our report. Immediate breast reconstruction can be performed in PABC after a careful selection....

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Chirappapha P, Thaweepworadej P, Ngamphaiboon N, et al. Breast reconstruction in pregnancy: a case report of multidisciplinary team approach in immediate autologous flap reconstruction for pregnancy-associated breast cancer. Clin Case Rep. 2017;5(9):1450-1453doi: 10.1002/ccr3.1092.
Chirappapha, P., Thaweepworadej, P., Ngamphaiboon, N., Sukprasert, M., Sukarayothin, T., & Leesombatpaiboon, M. (2017). Breast reconstruction in pregnancy: a case report of multidisciplinary team approach in immediate autologous flap reconstruction for pregnancy-associated breast cancer. Clinical case reports, 5(9), 1450-1453. https://doi.org/10.1002/ccr3.1092
Chirappapha, Prakasit, et al. "Breast reconstruction in pregnancy: a case report of multidisciplinary team approach in immediate autologous flap reconstruction for pregnancy-associated breast cancer." Clinical case reports vol. 5,9 (2017): 1450-1453. doi: https://doi.org/10.1002/ccr3.1092
Chirappapha P, Thaweepworadej P, Ngamphaiboon N, Sukprasert M, Sukarayothin T, Leesombatpaiboon M. Breast reconstruction in pregnancy: a case report of multidisciplinary team approach in immediate autologous flap reconstruction for pregnancy-associated breast cancer. Clin Case Rep. 2017 Jul 20;5(9):1450-1453. doi: 10.1002/ccr3.1092. eCollection 2017 Sep. PMID: 28878901; PMCID: PMC5582232.
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Serpentine supravenous hyperpigmentation.

Clinical case reports

Jamalpur I, Mogili HR, Koratala A.
PMID: 28878924
Clin Case Rep. 2017 Jul 25;5(9):1546-1547. doi: 10.1002/ccr3.1102. eCollection 2017 Sep.

Serpentine supravenous hyperpigmentation is a peculiar cutaneous eruption that follows the path of vein after intravenous injection of the chemotherapeutic agent. The lesions gradually resolve spontaneously if administration of the offending agent is stopped through the affected limb. Drugs...

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Jamalpur I, Mogili HR, Koratala A. Serpentine supravenous hyperpigmentation. Clin Case Rep. 2017;5(9):1546-1547doi: 10.1002/ccr3.1102.
Jamalpur, I., Mogili, H. R., & Koratala, A. (2017). Serpentine supravenous hyperpigmentation. Clinical case reports, 5(9), 1546-1547. https://doi.org/10.1002/ccr3.1102
Jamalpur, Indirakshi, et al. "Serpentine supravenous hyperpigmentation." Clinical case reports vol. 5,9 (2017): 1546-1547. doi: https://doi.org/10.1002/ccr3.1102
Jamalpur I, Mogili HR, Koratala A. Serpentine supravenous hyperpigmentation. Clin Case Rep. 2017 Jul 25;5(9):1546-1547. doi: 10.1002/ccr3.1102. eCollection 2017 Sep. PMID: 28878924; PMCID: PMC5582224.
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Diabetic ketoacidosis in vanishing white matter.

Clinical case reports

Alamri H, Al Mutairi F, Alothman J, Alothaim A, Alfadhel M, Alfares A.
PMID: 27525068
Clin Case Rep. 2016 Jun 17;4(8):717-20. doi: 10.1002/ccr3.597. eCollection 2016 Aug.

Clinicians should consider the EIF2B1 gene defect in any patient with diffuse white matter disease on an MRI of the brain and DKA.

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Alamri H, Al Mutairi F, Alothman J, et al. Diabetic ketoacidosis in vanishing white matter. Clin Case Rep. 2016;4(8):717-20doi: 10.1002/ccr3.597.
Alamri, H., Al Mutairi, F., Alothman, J., Alothaim, A., Alfadhel, M., & Alfares, A. (2016). Diabetic ketoacidosis in vanishing white matter. Clinical case reports, 4(8), 717-20. https://doi.org/10.1002/ccr3.597
Alamri, Hannadi, et al. "Diabetic ketoacidosis in vanishing white matter." Clinical case reports vol. 4,8 (2016): 717-20. doi: https://doi.org/10.1002/ccr3.597
Alamri H, Al Mutairi F, Alothman J, Alothaim A, Alfadhel M, Alfares A. Diabetic ketoacidosis in vanishing white matter. Clin Case Rep. 2016 Jun 17;4(8):717-20. doi: 10.1002/ccr3.597. eCollection 2016 Aug. PMID: 27525068; PMCID: PMC4974412.
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Blinatumomab may induce graft versus host leukemia in patients with pre-B ALL relapsing after hematopoietic stem cell transplant.

Clinical case reports

Khan MW, Gul Z.
PMID: 27525074
Clin Case Rep. 2016 Jun 24;4(8):743-6. doi: 10.1002/ccr3.604. eCollection 2016 Aug.

Blinatumomab, a bispecific T-cell engager monoclonal antibody used to manage Philadelphia chromosome-negative relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL) can be used to treat patients by inducing graft versus leukemia reaction post allogeneic hematopoietic stem cell transplantation,...

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Khan MW, Gul Z. Blinatumomab may induce graft versus host leukemia in patients with pre-B ALL relapsing after hematopoietic stem cell transplant. Clin Case Rep. 2016;4(8):743-6doi: 10.1002/ccr3.604.
Khan, M. W., & Gul, Z. (2016). Blinatumomab may induce graft versus host leukemia in patients with pre-B ALL relapsing after hematopoietic stem cell transplant. Clinical case reports, 4(8), 743-6. https://doi.org/10.1002/ccr3.604
Khan, Muhammad Waqas, and Gul, Zartash. "Blinatumomab may induce graft versus host leukemia in patients with pre-B ALL relapsing after hematopoietic stem cell transplant." Clinical case reports vol. 4,8 (2016): 743-6. doi: https://doi.org/10.1002/ccr3.604
Khan MW, Gul Z. Blinatumomab may induce graft versus host leukemia in patients with pre-B ALL relapsing after hematopoietic stem cell transplant. Clin Case Rep. 2016 Jun 24;4(8):743-6. doi: 10.1002/ccr3.604. eCollection 2016 Aug. PMID: 27525074; PMCID: PMC4974418.
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Association of a congenital long QT syndrome type 1 with Takotsubo cardiomyopathy.

Clinical case reports

El-Battrawy I, Behnes M, Borggrefe M, Akin I.
PMID: 27525086
Clin Case Rep. 2016 Jul 12;4(8):789-92. doi: 10.1002/ccr3.567. eCollection 2016 Aug.

The occurrence of takotsubo cardiomyopathy in a patient with congenital long QT syndrome has rarely been described. This case report discusses the occurrence of a clinically overt takotsubo cardiomyopathy accompanied by congenital long QT syndrome type 1 in a...

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El-Battrawy I, Behnes M, Borggrefe M, et al. Association of a congenital long QT syndrome type 1 with Takotsubo cardiomyopathy. Clin Case Rep. 2016;4(8):789-92doi: 10.1002/ccr3.567.
El-Battrawy, I., Behnes, M., Borggrefe, M., & Akin, I. (2016). Association of a congenital long QT syndrome type 1 with Takotsubo cardiomyopathy. Clinical case reports, 4(8), 789-92. https://doi.org/10.1002/ccr3.567
El-Battrawy, Ibrahim, et al. "Association of a congenital long QT syndrome type 1 with Takotsubo cardiomyopathy." Clinical case reports vol. 4,8 (2016): 789-92. doi: https://doi.org/10.1002/ccr3.567
El-Battrawy I, Behnes M, Borggrefe M, Akin I. Association of a congenital long QT syndrome type 1 with Takotsubo cardiomyopathy. Clin Case Rep. 2016 Jul 12;4(8):789-92. doi: 10.1002/ccr3.567. eCollection 2016 Aug. PMID: 27525086; PMCID: PMC4974430.
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GM-CSF as successful salvage therapy of metamizole (dipyrone)-induced agranulocytosis with Fournier's gangrene and severe septic shock in an adolescent.

Clinical case reports

Winkler A, Kietz S, Bahlmann H, Jafarzade G, Lode HN, Heckmann M.
PMID: 27525093
Clin Case Rep. 2016 Jul 20;4(8):816-9. doi: 10.1002/ccr3.616. eCollection 2016 Aug.

This case report describes the successful use of granulocyte and macrophage colony-stimulating factor as salvage therapy and an alternative to hematopoietic stem cell transplantation in a 14-year-old adolescent with metamizole (dipyrone)-induced agranulocytosis and severe septic shock.

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Winkler A, Kietz S, Bahlmann H, et al. GM-CSF as successful salvage therapy of metamizole (dipyrone)-induced agranulocytosis with Fournier's gangrene and severe septic shock in an adolescent. Clin Case Rep. 2016;4(8):816-9doi: 10.1002/ccr3.616.
Winkler, A., Kietz, S., Bahlmann, H., Jafarzade, G., Lode, H. N., & Heckmann, M. (2016). GM-CSF as successful salvage therapy of metamizole (dipyrone)-induced agranulocytosis with Fournier's gangrene and severe septic shock in an adolescent. Clinical case reports, 4(8), 816-9. https://doi.org/10.1002/ccr3.616
Winkler, Annegret, et al. "GM-CSF as successful salvage therapy of metamizole (dipyrone)-induced agranulocytosis with Fournier's gangrene and severe septic shock in an adolescent." Clinical case reports vol. 4,8 (2016): 816-9. doi: https://doi.org/10.1002/ccr3.616
Winkler A, Kietz S, Bahlmann H, Jafarzade G, Lode HN, Heckmann M. GM-CSF as successful salvage therapy of metamizole (dipyrone)-induced agranulocytosis with Fournier's gangrene and severe septic shock in an adolescent. Clin Case Rep. 2016 Jul 20;4(8):816-9. doi: 10.1002/ccr3.616. eCollection 2016 Aug. PMID: 27525093; PMCID: PMC4974437.
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An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature.

Clinical case reports

Õunap K, Pajusalu S, Zilina O, Reimand T, Žordania R.
PMID: 27525095
Clin Case Rep. 2016 Jul 22;4(8):824-30. doi: 10.1002/ccr3.632. eCollection 2016 Aug.

3q26.33-3q27.2 microdeletion can be classified as a clinical entity characterized by intrauterine growth retardation, feeding problems in infancy, short stature, intellectual disability, hypotonia, dysmorphic facial features (medially sparse eyebrows, narrow horizontal palpebral fissures, epicanthal folds, flat nasal bridge and...

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Õunap K, Pajusalu S, Zilina O, et al. An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature. Clin Case Rep. 2016;4(8):824-30doi: 10.1002/ccr3.632.
Õunap, K., Pajusalu, S., Zilina, O., Reimand, T., & Žordania, R. (2016). An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature. Clinical case reports, 4(8), 824-30. https://doi.org/10.1002/ccr3.632
Õunap, Katrin, et al. "An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature." Clinical case reports vol. 4,8 (2016): 824-30. doi: https://doi.org/10.1002/ccr3.632
Õunap K, Pajusalu S, Zilina O, Reimand T, Žordania R. An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature. Clin Case Rep. 2016 Jul 22;4(8):824-30. doi: 10.1002/ccr3.632. eCollection 2016 Aug. PMID: 27525095; PMCID: PMC4974439.
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A kidney-shaped polycystic mass on the back of a hemodialysis patient.

Clinical case reports

Volkmann J, Nordlohne J, Schmitt R, von Vietinghoff S.
PMID: 27525098
Clin Case Rep. 2016 Jul 06;4(8):840-1. doi: 10.1002/ccr3.627. eCollection 2016 Aug.

Multicystic back masses can be of infectious, metastatic, or local pre- or malignant origin. We present a case of a rapidly evolving mass in a hemodialysis patient with severe "chronic kidney disease-associated mineral bone disease" (CKD-MBD), that also highlights...

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Volkmann J, Nordlohne J, Schmitt R, et al. A kidney-shaped polycystic mass on the back of a hemodialysis patient. Clin Case Rep. 2016;4(8):840-1doi: 10.1002/ccr3.627.
Volkmann, J., Nordlohne, J., Schmitt, R., & von Vietinghoff, S. (2016). A kidney-shaped polycystic mass on the back of a hemodialysis patient. Clinical case reports, 4(8), 840-1. https://doi.org/10.1002/ccr3.627
Volkmann, Julia, et al. "A kidney-shaped polycystic mass on the back of a hemodialysis patient." Clinical case reports vol. 4,8 (2016): 840-1. doi: https://doi.org/10.1002/ccr3.627
Volkmann J, Nordlohne J, Schmitt R, von Vietinghoff S. A kidney-shaped polycystic mass on the back of a hemodialysis patient. Clin Case Rep. 2016 Jul 06;4(8):840-1. doi: 10.1002/ccr3.627. eCollection 2016 Aug. PMID: 27525098; PMCID: PMC4974442.
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Atrial mass: a myxoma?.

Clinical case reports

Chatzis AC, Kostopanagiotou K, Kousi T, Mitropoulos F.
PMID: 27525099
Clin Case Rep. 2016 Jul 13;4(8):842-3. doi: 10.1002/ccr3.626. eCollection 2016 Aug.

A middle-aged woman with a history of resected colorectal cancer and receiving chemotherapy presented with a right atrial mass and the provisional diagnosis of myxoma supported by echocardiography, computed tomography, and magnetic resonance imaging. Successful surgical removal revealed organized...

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Chatzis AC, Kostopanagiotou K, Kousi T, et al. Atrial mass: a myxoma?. Clin Case Rep. 2016;4(8):842-3doi: 10.1002/ccr3.626.
Chatzis, A. C., Kostopanagiotou, K., Kousi, T., & Mitropoulos, F. (2016). Atrial mass: a myxoma?. Clinical case reports, 4(8), 842-3. https://doi.org/10.1002/ccr3.626
Chatzis, Andrew C, et al. "Atrial mass: a myxoma?." Clinical case reports vol. 4,8 (2016): 842-3. doi: https://doi.org/10.1002/ccr3.626
Chatzis AC, Kostopanagiotou K, Kousi T, Mitropoulos F. Atrial mass: a myxoma?. Clin Case Rep. 2016 Jul 13;4(8):842-3. doi: 10.1002/ccr3.626. eCollection 2016 Aug. PMID: 27525099; PMCID: PMC4974443.
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An HCV-positive recipient of an HCV-positive donor liver successfully treated before and immediately after liver transplant with daclatasvir, sofosbuvir, and ribavirin.

Clinical case reports

Poordad F, Lawitz E, Gutierrez JA, Guerrero J, Speeg K, Swenson ES.
PMID: 28396749
Clin Case Rep. 2017 Feb 03;5(4):371-375. doi: 10.1002/ccr3.841. eCollection 2017 Apr.

This case suggests that initiation of HCV therapy immediately after liver transplantation with well-tolerated, all-oral regimens may achieve a virologic cure in HCV-positive recipients, thus preventing post-transplant HCV recurrence and associated disease progression. This strategy may broaden utilization of...

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Poordad F, Lawitz E, Gutierrez JA, et al. An HCV-positive recipient of an HCV-positive donor liver successfully treated before and immediately after liver transplant with daclatasvir, sofosbuvir, and ribavirin. Clin Case Rep. 2017;5(4):371-375doi: 10.1002/ccr3.841.
Poordad, F., Lawitz, E., Gutierrez, J. A., Guerrero, J., Speeg, K., & Swenson, E. S. (2017). An HCV-positive recipient of an HCV-positive donor liver successfully treated before and immediately after liver transplant with daclatasvir, sofosbuvir, and ribavirin. Clinical case reports, 5(4), 371-375. https://doi.org/10.1002/ccr3.841
Poordad, Fred, et al. "An HCV-positive recipient of an HCV-positive donor liver successfully treated before and immediately after liver transplant with daclatasvir, sofosbuvir, and ribavirin." Clinical case reports vol. 5,4 (2017): 371-375. doi: https://doi.org/10.1002/ccr3.841
Poordad F, Lawitz E, Gutierrez JA, Guerrero J, Speeg K, Swenson ES. An HCV-positive recipient of an HCV-positive donor liver successfully treated before and immediately after liver transplant with daclatasvir, sofosbuvir, and ribavirin. Clin Case Rep. 2017 Feb 03;5(4):371-375. doi: 10.1002/ccr3.841. eCollection 2017 Apr. PMID: 28396749; PMCID: PMC5378822.
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Showing 1 to 12 of 5409 entries