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Genotype-Phenotype Correlations in Neurofibromatosis and Their Potential Clinical Use

Neurology, 2021-08, Vol.97 (7 Suppl 1), p.S91

2021

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Role of NF2 Haploinsufficiency in NF2-associated Polyneuropathy

Brain pathology (Zurich, Switzerland), 2007-10, Vol.17 (4), p.371-376

2007

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Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD

Annals of neurology, 2005-11, Vol.58 (5), p.777-780

2005

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Activation of ERK, AKT and JNK signalling pathways in human schwannomas in situ

Histopathology, 2009-12, Vol.55 (6), p.744-749

2009

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Expression of c-Jun and Sox-2 in human schwannomas and traumatic neuromas

Histopathology, 2013-03, Vol.62 (4), p.651-656

2013

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Conclusions and future directions for the REiNS International Collaboration

Neurology, 2013-11, Vol.81 (21 Suppl 1), p.S41

2013

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PAK kinase regulates Rac GTPase and is a potential target in human schwannomas

Experimental neurology, 2009-07, Vol.218 (1), p.137-144

2009

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Constitutive activation of the EGFR–STAT1 axis increases proliferation of meningioma tumor cells

Neuro-oncology advances, 2020-01, Vol.2 (1), p.vdaa008-vdaa008

2020

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Low affinity NGF receptor expression in CMT1A nerve biopsies of different disease stages

Brain (London, England : 1878), 1996-10, Vol.119 (5), p.1461-1469

1996

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Abstract 2609: The role of focal adhesion kinase (FAK), PI3K/AKT and p53/mouse double minute 2 homologue (MDM2) complex in the pathobiology of Merlin-deficient tumors

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.2609-2609

2014

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Abstract 704: Scaffold protein KSR1 is negatively regulated by merlin and promotes tumor development in merlin deficient tumors

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.704-704

2015

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Expression of c‐ J un and S ox‐2 in human schwannomas and traumatic neuromas

Histopathology, 2013-03, Vol.62 (4), p.651-656

2013

Volltextzugriff (PDF)

Clinical trials in pediatric ALS: a TRICALS feasibility study

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2022, Vol.23 (7-8), p.481-488

2022

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Hereditary motor neuropathies and motor neuron diseases: which is which

Amyotrophic lateral sclerosis, 2002, Vol.3 (4), p.186-189

2002

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Low affinity NGF receptor expression in CMT1 A nerve biopsies of different disease stages

Brain (London, England : 1878), 1996-10, Vol.119 (5), p.1461-1469

1996

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Neuroligand-mediated calcium signaling in cultured human schwannoma cells

Journal of the peripheral nervous system, 1999, Vol.4 (2), p.99-105

1999

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Molecular and translational advances in meningiomas

Neuro-oncology (Charlottesville, Va.), 2019-01, Vol.21 (Supplement_1), p.i4-i17

2019

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Nilotinib alone or in combination with selumetinib is a drug candidate for neurofibromatosis type 2

Neuro-oncology (Charlottesville, Va.), 2011-07, Vol.13 (7), p.759-766

2011

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Actin-Rich Protrusions and Nonlocalized GTPase Activation in Merlin-Deficient Schwannomas

Journal of neuropathology and experimental neurology, 2007-07, Vol.66 (7), p.608-616

2007

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A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia‐like phenotype of Tangier disease

Brain (London, England : 1878), 2003-04, Vol.126 (4), p.920-927

2003

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Spinal Neurofibromatosis without Café-au-Lait Macules in Two Families with Null Mutations of the NF1 Gene

American journal of human genetics, 2001-12, Vol.69 (6), p.1395-1400

2001

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Quinidine impairs proliferation of neurofibromatosis type 2‐deficient human malignant mesothelioma cells

Cancer, 2003-04, Vol.97 (8), p.1955-1962

2003

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Genotype-Phenotype Correlations in Neurofibromatosis and Their Potential Clinical Use

Role of NF2 Haploinsufficiency in NF2-associated Polyneuropathy

Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD

Activation of ERK, AKT and JNK signalling pathways in human schwannomas in situ

Expression of c-Jun and Sox-2 in human schwannomas and traumatic neuromas

Conclusions and future directions for the REiNS International Collaboration

PAK kinase regulates Rac GTPase and is a potential target in human schwannomas

Constitutive activation of the EGFR–STAT1 axis increases proliferation of meningioma tumor cells

Low affinity NGF receptor expression in CMT1A nerve biopsies of different disease stages

Abstract 2609: The role of focal adhesion kinase (FAK), PI3K/AKT and p53/mouse double minute 2 homologue (MDM2) complex in the pathobiology of Merlin-deficient tumors

Abstract 704: Scaffold protein KSR1 is negatively regulated by merlin and promotes tumor development in merlin deficient tumors

Expression of c‐ J un and S ox‐2 in human schwannomas and traumatic neuromas

Clinical trials in pediatric ALS: a TRICALS feasibility study

Hereditary motor neuropathies and motor neuron diseases: which is which

Low affinity NGF receptor expression in CMT1 A nerve biopsies of different disease stages

Neuroligand-mediated calcium signaling in cultured human schwannoma cells

Molecular and translational advances in meningiomas

Nilotinib alone or in combination with selumetinib is a drug candidate for neurofibromatosis type 2

Actin-Rich Protrusions and Nonlocalized GTPase Activation in Merlin-Deficient Schwannomas

A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia‐like phenotype of Tangier disease

Spinal Neurofibromatosis without Café-au-Lait Macules in Two Families with Null Mutations of the NF1 Gene

Quinidine impairs proliferation of neurofibromatosis type 2‐deficient human malignant mesothelioma cells

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