[PDF] Top 20 Topological properties of sand automata as cellular automata
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Precocious puberty in Turner Syndrome: report of a case and review of the literature
... spontaneous puberty has been reported with a significantly higher frequency among mosaic TS with cell lines having more than one ...spontaneous puberty [18]. In keeping with this, our case suggests ... See full document
178
Brittle cornea syndrome: a case report and review of the literature
... this case report and review of the literature, we aim to highlight the importance in the diagnosis and treatment of patients suffered from this ... See full document
59
Case Report Posterior reversible encephalopathy syndrome in a child with steroid-resistant nephrotic syndrome: a case report and review of literature
... encephalopathy syndrome, a rare disorder of central nervous system, was first described by Hinchey in 1996 ...a case of PRES in a 12-year-old girl with steroid-resistant nephrotic ... See full document
73
Case Report Concurrent bilateral testicular hamartomas and serous borderline tumors in a patient with complete androgen insensitivity syndrome: a case report and review of the literature
... Gonadal neoplasms are the main concern in CAIS patients, especially malignant germ cell tumors. The risk of neoplastic development was considered high previously [11, 12], but recent reports suggest only small number of ... See full document
177
Tetrasomy 18p: case report and review of literature
... this syndrome at the phenotypic level has been scarce in the ...this report, we present de novo tetrasomy 18p in a male Saudi baby featuring cerebellar and renal mal- formations, in addition to the typical ... See full document
11
Liver transplantation for a patient with Turner syndrome presenting severe portal hypertension: a case report and literature review
... Background: Liver involvement in Turner syndrome (TS) patients has been more clearly clarified in recent years. Most of the clinical manifestations in TS are asymptomatic and can be detected as liver test ... See full document
13
Pheochromocytoma as a rare cause of hypertension in a 46 X, i(X)(q10) turner syndrome: a case report and literature review
... Laboratory tests revealed a fasting glucose level of 88 mg/dL, HbA1C 4.8%, C-peptide 6.34 ng /mL(reference range, 0.4–4 ng/mL), and anti-glutamate decarboxylase (GAD) antibody < 0.5 U/mL(reference range, 0–1.0 U/mL). ... See full document
7
Case Report Pathological diagnosis of a rare intestinal penicillium marneffei infection in an acquired immunodeficiency syndrome patient: a case report and literature review
... this report, we presented a rare case of an HIV-infected Chinese patient with intestinal penicilliosis marneffei, who was characterized by an insidious onset, initial symptoms with a mild pain in the lower ... See full document
161
Management of intrahepatic splenosis:a case report and review of the literature
... In fact, most of the cases with intrahepatic splenosis that had been reported were treated with invasive proce- dures, including biopsy and surgical resection. However, intrahepatic splenosis may be beneficial in the ... See full document
95
A case report and literature review of primary resistant Hodgkin lymphoma: a response to anti-PD-1 after failure of autologous stem cell transplantation and brentuximab vedotin
... This case report presents the case of a 54-year-old patient with primary resistant HL who received single-agent treatment, brentuximab vedotin, after ASCT ...This case provides support for a ... See full document
7
<p>Lemierre Syndrome. A Forgotten Disease. Case Report and Review of Literature</p>
... Discussion: Lemierre syndrome is most frequently caused by the anaerobic bacterium, Fusobacterium necrophorum. Although rare, there is evidence of a resurgence in the condi- tion in recent years, most probably due ... See full document
5
Warfarin-induced calciphylaxis: a case report and review of literature
... Abstract: Calciphylaxis is a challenging complication of end-stage renal disease, with an unknown underlying mechanism. Several risk factors have been identified, such as hyper- phosphatemia, hypercalcemia, ... See full document
10
Binder’s Syndrome – A Rare Case Report and Review of Literature with Detailed Treatment Plan
... Binder’s syndrome (also known as maxillofacial hypoplasia) is characterized by hypoplasia of the nasomaxillary ...Binder’s syndrome. The syndrome is quite rare, which may be a reason for the lack of ... See full document
29
Capsular block syndrome: a case report and literature review
... Results: A 69-year-old patient complained of decreased visual acuity 11 months after undergo- ing phacoemulsification. She was found to have a secondary myopization. Anterior segment ultrabiomicroscopy confirmed the ... See full document
11
Optic glioma and precocious puberty in a girl with neurofibromatosis type 1 carrying an R681X mutation of NF1: case report and review of the literature
... Association of NF1 with optic glioma or precocious puberty is not rare, but has rarely been molecularly charac- terized [13, 14, 17–19]. Among 20 patients with optic glioma, NF1 mutations were detected in ... See full document
5
Case Report A rare case of Turner syndrome with a special karyotype: a case report and review of literature
... At first, it was believed that the short arm of the X-chromosome was associated with short stat- ure, and the long arm of the X-chromosome was related with ovarian dysgenesis [17]. However, only homeobox gene (Shox) ... See full document
129
Ameloblastoma: Report of two Cases and A Brief Literature Review
... Although a wide variation in the range of ages can be observed, ameloblastoma primarily affects young adults between the fourth and fifth decades of life. Unlike the observation in the first case report ... See full document
7
Precocious Puberty Associated with an Adrenal Tumor: A case report
... Precocious puberty with or without Cushing syndrome ...pseudoprecocious puberty. Other cases in the literature were also reviewed to raise awareness of potential diagnosis of ... See full document
32
Precocious puberty and Chiari I malformation with syrinx: a case report of an unusual presentation of Costello syndrome
... As CPP is rare in CS, we propose children with CS presenting with borderline precocious puberty receive brain MRI. A 2003 literature review revealed 73.7% of CS patients receiving MRI ... See full document
11
A case of acute Sheehan’s syndrome and literature review: a rare but life threatening complication of postpartum hemorrhage
... Sheehan’s syndrome was first described by Sheehan in 1937 [4]; through improved management of hemodynamic complications, its incidence has gradually declined over ...Sheehan’s syndrome is pituitary necrosis ... See full document
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