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    Academic Journals

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• Basal like carcinoma of breast in patient with neurofibromatosis I: An association or co-existence?

  Authors:Sree Jinkala, Nachiappa Rajesh, and Arvind RamkumarFrom:Indian Journal of Pathology and Microbiology (Vol. 56, Issue 2) Peer-Reviewed

  April-June 20131,245 words Article 1830LByline: Sree. Jinkala, Nachiappa. Rajesh, Arvind. Ramkumar Neurofibromatosis I (NF I), an autosomal dominant disorder is associated with increased risk of benign and malignant peripheral nerve sheath tumors and...

• Cranio-orbital-temporal neurofibromatosis: An uncommon subtype of neurofibromatosis type-1

  Authors:Nibedita Acharya, Manjoo Reddy, Caroline Paulson, and Deepti PrasannaFrom:Oman Journal of Ophthalmology (Vol. 7, Issue 1) Peer-Reviewed

  January-April 2014673 words Clinical report 1460LByline: Nibedita. Acharya, Manjoo. Reddy, Caroline. Paulson, Deepti. Prasanna Introduction Neurofibromatosis is a multisystem genetic disorder that is commonly associated with cutaneous, neurologic, ophthalmic,...

• Malignant peripheral nerve sheath tumor of adrenal gland with heterologus osseous differentiation in a case of Von Recklinghausen's disease

  Authors:Manas Baisakh, Nachiketa Mohapatra, Samiran Adhikary, and Debasis RoutrayFrom:Indian Journal of Pathology and Microbiology (Vol. 57, Issue 1) Peer-Reviewed

  January-March 20141,407 words Clinical report 1520LByline: Manas. Baisakh, Nachiketa. Mohapatra, Samiran. Adhikary, Debasis. Routray Malignant peripheral nerve sheath tumor (MPNST) of the adrenal gland is extremely rare. Most of them occur in association with...

• Segmental schwannomatosis: An uncommon cause of crural monoparesis

  Authors:Ajith Cherian, Neeraj Baheti, C. Sarada, Thomas Iype, and Mini MathewFrom:Journal of Neurosciences in Rural Practice (Vol. 3, Issue 3) Peer-Reviewed

  September-December 2012740 words Report 1640LByline: Ajith. Cherian, Neeraj. Baheti, C. Sarada, Thomas. Iype, Mini. Mathew Schwannomas are nerve tumors that occur in three clinical settings - as localized schwannomas, as a part of Von Recklinghausen syndrome,...

• Transvaginal evisceration after laparoscopic adrenalectomy in neurofibromatosis

  Authors:Nereo Vettoretto, Luca Balestra, Lucio Taglietti, and Maurizio GiovanettiFrom:Journal of Emergencies, Trauma, and Shock (Vol. 3, Issue 2) Peer-Reviewed

  April-June 20101,194 words Report Byline: Nereo. Vettoretto, Luca. Balestra, Lucio. Taglietti, Maurizio. Giovanetti Transvaginal evisceration is a rare complication of hysterectomy. We describe this event following adrenalectomy for pheochromocytoma...

• Auditory brainstem implantation: The first Indian experience

  Authors:Mohan Kameswaran, M. Vasudevan, R. Anand Kumar, Jawahar Nagasundaram, Kiran Natarajan, and S. RaghunandhanFrom:Indian Journal of Otolaryngology and Head and Neck Surgery (Vol. 57, Issue 1) Peer-Reviewed

  January-March 20052,966 words Article Byline: Mohan. Kameswaran, M. Vasudevan, R. Anand Kumar, Jawahar. Nagasundaram, Kiran. Natarajan, S. Raghunandhan Multichannel auditory brainstem implants (ABI) are currently indicated for patients with...

• Multiple mirror image cervical neurofibromas in neurofibromatosis type 1

  Authors:Saraj Singh, Dipankar Mankotia, Sachin Borkar, and Uditi GuptaFrom:Neurology India (Vol. 65, Issue 2) Peer-Reviewed

  March-April 2017413 words Report 1490LByline: Saraj. Singh, Dipankar. Mankotia, Sachin. Borkar, Uditi. Gupta An autosomal dominant disorder, neurofibromatosis-1 (NF1) has different forms of presentation in adolescents. Here, the author is reporting a...

• Successful surgical management of bilateral epiretinal membrane in a child with only cafe-au-lait spots

  Authors:Swetha Philip, Thomas Kuriakose, and Geeta ChackoFrom:Indian Journal of Ophthalmology (Vol. 65, Issue 6) Peer-Reviewed

  June 20171,424 words Article 1750LByline: Swetha. Philip, Thomas. Kuriakose, Geeta. Chacko A 6-year-old boy diagnosed as anisometropic amblyopia, with only cafe-au-lait spots and a family history of neurofibromatosis, presented with decrease in...

• Intraparotid neurofibromatosis presenting with multiple nodules

  Authors:Ryan F. Osborne, Jason S. Hamilton, and Reena GuptaFrom:Ear, Nose and Throat Journal (Vol. 92, Issue 6) Peer-Reviewed

  June 2013618 words Case study 1180LNeurofibroma of the parotid gland is extremely rare. When it does occur, it usually does so in patients with neurofibromatosis type 1 (NF-1). We describe a case of intraparotid neurofibromatosis that was even more...

• Recurrent hematochezia secondary to gastrointestinal stromal tumors (GISTs) in neurofibromatosis type one

  Authors:Justin T. Kupec, H. James Williams, Andrew K. Roorda, and Stephan U. GoebelFrom:West Virginia Medical Journal (Vol. 107, Issue 4) Peer-Reviewed

  July-August 20112,187 words Case study 1600LAbstract Background: Patients with neurofibromatosis type 1 (NF1) suffer from cutaneous, neurological and intestinal complications due to the mutation of the neurofibromin gene and abnormal protein product....

• STENOTIC AORTO-ARTERIOPATHY IN A TWENTY MONTH OLD MALE

  Authors:Arabella C. Stock, J. Glickstein, G. Crooke, and J. Weingarten-AramsFrom:Chest (Vol. 116, Issue 4) Peer-Reviewed

  Oct. 1999990 words Abstract Introduction: Stenotic aorto-arteriopathy (SAA) is a constellation of uncommon vascular diseases characterized by segmental stenosis of the aorta and its branches. Etiologies of SAA include Takayasu's arteritis (TA),...

• Bilateral Diaphragm Paralysis Secondary to Central von Recklinghausen's Disease(*)

  Authors:Paul M. Hassoun and Bartolome R. CelliFrom:Chest (Vol. 117, Issue 4) Peer-Reviewed

  Apr. 20001,637 words Article Bilateral paralysis of the diaphragm is either idiopathic or associated with several medical conditions, including trauma or thoracic surgery, viral infections, and neurologic congenital or degenerative disorders. We...

• Tuberous Sclerosis Complex: State-of-the-Art Review with a Focus on Pulmonary Involvement

  Authors:Felipe Mussi von Ranke, Glaucia Zanetti, Jorge Luiz Pereira e Silva, Cesar Augusto Araujo Neto, Myrna C. B. Godoy, Carolina A. Souza, et al.From:Lung (Vol. 193, Issue 5) Peer-Reviewed

  Oct. 20155,855 words Report 1330LTuberous sclerosis complex (TSC) is an autosomal-dominant neurocutaneous disease with high phenotypic variability. The incidence is approximately one in 5000-10,000 births. TSC is characterized by widespread hamartomas...

• Cruveilhier and acoustic neuroma

  Author:JMS PearceFrom:Journal of Neurology, Neurosurgery and Psychiatry (Vol. 74, Issue 8) Peer-Reviewed

  Aug. 2003589 words Article Some 20 years after the first observations published on neuromas (William Wood in 1828), (1) Robert William Smith published his treatise on neuromas, (2) which included a full description of von Recklinghausen's...

• MEK inhibition exhibits efficacy in human and mouse neurofibromatosis tumors

  Authors:Walter J. Jessen, Shyra J. Miller, Edwin Jousma, Jianqiang Wu, Tilat A. Rizvi, Meghan E. Brundage, et al.From:Journal of Clinical Investigation (Vol. 123, Issue 1) Peer-Reviewed

  Jan. 20136,250 words Report 1360LNeurofibromatosis type 1 (NF1) patients develop benign neurofibromas and malignant peripheral nerve sheath tumors (MPNST). These incurable peripheral nerve tumors result from loss of NF1 tumor suppressor gene function,...

• Selection of internal references for RT-qPCR assays in Neurofibromatosis type 1 (NF1) related Schwann cell lines

  Authors:Yi-Hui Gu, Xi-Wei Cui, Jie-Yi Ren, Man-Mei Long, Wei Wang, Cheng-Jiang Wei, et al.From:PLoS ONE (Vol. 16, Issue 2) Peer-Reviewed

  Feb. 25, 20215,277 words Report 1470LReal-time quantitative PCR (RT-qPCR) has been widely applied in uncovering disease mechanisms and screening potential biomarkers. Internal reference gene selection determines the accuracy and reproducibility of data...

• T-lineage acute lymphoblastic leukemia and parvovirus infection in a child with neurofibromastosis-1

  Authors:Pallavi Agarwal, Shano Naseem, Neelam Varma, and R. MarwahaFrom:Indian Journal of Pathology and Microbiology (Vol. 56, Issue 4) Peer-Reviewed

  October-December 20131,961 words Case study 1440LByline: Pallavi. Agarwal, Shano. Naseem, Neelam. Varma, R. Marwaha Neurofibromatosis (NF-1) patients have an increased risk of developing malignancies most commonly rhabdomyosarcomas, optic gliomas, brain tumors and...

• Commentary

  Author:Keerati HongsakulFrom:Journal of Neurosciences in Rural Practice (Vol. 5, Issue 3) Peer-Reviewed

  July-September 2014565 words Report 1450LByline: Keerati. Hongsakul Neurofibromatosis type 1 (NF1), or Von Recklinghausen disease, is a group of heterogeneous diseases that present with multiorgan involvement. This disease is an autosomal dominant genetic...

• Oral hamartomas with von Recklinghausen disease

  Authors:C. Kumar, R. Jagat Reddy, Siddarth Gupta, and Sanjeev LallerFrom:Annals of Saudi Medicine (Vol. 31, Issue 4) Peer-Reviewed

  July-August 20111,570 words Case study 1540LByline: C. Kumar, R. Jagat Reddy, Siddarth. Gupta, Sanjeev. Laller Neurofibromatosis is a genetically-inherited disorder of the nervous system that primarily affects the development and growth of neural (nerve) cell...

• Spontaneous rupture of adrenal pheochromocytoma in a patient with Von Recklinghausen's disease

  Authors:Ramin Azhough, Ali Barband, Negar Motayagheni, Mitra Niafar, and Hojjat PourfathiFrom:Indian Journal of Critical Care Medicine (Vol. 13, Issue 2) Peer-Reviewed

  April-June 20091,022 words Case study Byline: Ramin. Azhough, Ali. Barband, Negar. Motayagheni, Mitra. Niafar, Hojjat. Pourfathi Spontaneous rupture of an adrenal pheochromocytoma is extremely rare and can be lethal because of dramatic changes in the...