F.H.M. Grapperhaus, Alva en de tiende penning oleh F.R. Postma

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Hegemoni Metroseksual dalam Iklan Grooming di Majalah FHM Indonesia oleh Nobertus Ribut Santoso

"…Abstract: This research is derived from a formulation of how FHM Indonesia magazine conducts metrosexual hegemony through grooming advertisements. …"
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F.H.M. Grapperhaus, Alva en de tiende penning oleh F.R. Postma

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F.H.M. Grapperhaus, Alva en de tiende penning oleh F.R. Postma

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F.H.M. Grapperhaus, Alva en de tiende penning oleh F.R. Postma

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First FHM3 mouse model shows spontaneous cortical spreading depolarizations oleh Nico A. Jansen, Anisa Dehghani, Margot M. L. Linssen, Cor Breukel, Else A. Tolner, Arn M. J. M. van denMaagdenberg

"…Abstract Here we show, for the first time, spontaneous cortical spreading depolarization (CSD) events – the electrophysiological correlate of the migraine aura – in animals by using the first generated familial hemiplegic migraine type 3 (FHM3) transgenic mouse model. The mutant mice express L263V‐mutated α1 subunits in voltage‐gated NaV1.1 sodium channels (Scn1aL263V). …"
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A homolog of FHM2 is involved in modulation of excitatory neurotransmission by serotonin in C. elegans. oleh Elena G Govorunova, Mustapha Moussaif, Andrey Kullyev, Ken C Q Nguyen, Thomas V McDonald, David H Hall, Ji Y Sze

"…The C. elegans eat-6 gene encodes a Na(+), K(+)-ATPase alpha subunit and is a homolog of the familial hemiplegic migraine candidate gene FHM2. Migraine is the most common neurological disorder linked to serotonergic dysfunction. …"
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Comparing Reliability of FHM and ISA Methods in Assessing Old and Large Dipterocarp Trees Health oleh Arief Noor Rachmadiyanto, Lina Karlinasari, Dodi Nandika, Joko Ridho Witono, Iskandar Zulkarnaen Siregar

"…Abstract Forest Health Monitoring (FHM) and International Society of Arboriculture (ISA) methods are used for individual tree health assessment. …"
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Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM families oleh Luciana R. Lopes, Mario Fernando Prieto Peres, Kaate R.J. Vanmolkot, Patrícia R. Tobo, Eliova Zukerman, Rune R. Frants, Arn M.J.M. van den Maagdenberg, Carlos Alberto Moreira-Filho

"…Familial hemiplegic migraine (FHM) is a rare autosomal dominant form of migraine with aura. …"
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Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report oleh Na Shao, Haining Zhang, Xue Wang, Wuqiong Zhang, Miaomiao Yu, Hongmei Meng

"…The familial hemiplegic migraine type 3 (FHM3) is seldom caused by mutations in SCN1A. Here, we report a rare case of an SCN1A mutation leading to FHM3 in a Chinese family. …"
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Neurovascular changes in magnetic resonance imagining and single-photon emission computed tomography during migraine attack in patients with FHM2 mutations oleh Azusa Nagai, Daiki Tanaka, Kiyomi Kuroshima, Shigehisa Ura, Kazuto Yoshida, Yuji Takahashi, Ichiro Yabe

"…Both patients were diagnosed with FHM2 (p.R763H mutation in ATP1A2 ). This study highlights the importance of neurovascular examinations during the FHM2 headache phase. …"
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A Fusion-Based Technique With Hybrid Swarm Algorithm and Deep Learning for Biosignal Classification oleh Sunil Kumar Prabhakar, Harikumar Rajaguru, Chulho Kim, Dong-Ok Won

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First Attack and Clinical Presentation of Hemiplegic Migraine in Pediatric Age: A Multicenter Retrospective Study and Literature Review oleh Irene Toldo, Francesco Brunello, Veronica Morao, Egle Perissinotto, Massimiliano Valeriani, Dario Pruna, Elisabetta Tozzi, Filomena Moscano, Giovanni Farello, Roberto Frusciante, Marco Carotenuto, Carlo Lisotto, Silvia Ruffatti, Ferdinando Maggioni, Cristiano Termine, Gabriella Di Rosa, Margherita Nosadini, Stefano Sartori, Pier Antonio Battistella

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PENILAIAN KESEHATAN TAHURA BANTEN PADA BLOK KOLEKSI TUMBUHAN DAN ATAU SATWA oleh Nur Rohman, Rahmat Safe’i, Slamet Budi Yuwono, Gunardi Djoko Winanrno, Sugeng P. Harianto, Agus Setiawan

Subjek: "…FHM; Kesehatan Hutan; Status; Tahura Banten…"
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Cerebellar Atrophy and Changes in Cytokines Associated with the CACNA1A R583Q Mutation in a Russian Familial Hemiplegic Migraine Type 1 Family oleh Svetlana F. Khaiboullina, Elena G. Mendelevich, Leyla H. Shigapova, Elena Shagimardanova, Guzel Gazizova, Alexey Nikitin, Ekaterina Martynova, Yuriy N. Davidyuk, Enver I. Bogdanov, Oleg Gusev, Oleg Gusev, Oleg Gusev, Arn M. J. M. van den Maagdenberg, Rashid A. Giniatullin, Rashid A. Giniatullin, Albert A. Rizvanov

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Serial magnetic resonance imaging findings during severe attacks of familial hemiplegic migraine type 2: a case report oleh David Fear, Misha Patel, Ramin Zand

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Aura and Stroke: relationship and what we have learnt from preclinical models oleh Muge Yemisci, Katharina Eikermann-Haerter

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A Novel Estimation of the Composite Hazard of Landslides and Flash Floods Utilizing an Artificial Intelligence Approach oleh Mohamed Wahba, Mustafa El-Rawy, Nassir Al-Arifi, Mahmoud M. Mansour

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The mechanism of functional up-regulation of P2X3 receptors of trigeminal sensory neurons in a genetic mouse model of familial hemiplegic migraine type 1 (FHM-1). oleh Swathi K Hullugundi, Michel D Ferrari, Arn M J M van den Maagdenberg, Andrea Nistri

"…A knock-in (KI) mouse model of FHM-1 expressing the R192Q missense mutation of the Cacna1a gene coding for the α1 subunit of CaV2.1 channels shows, at the level of the trigeminal ganglion, selective functional up-regulation of ATP -gated P2X3 receptors of sensory neurons that convey nociceptive signals to the brainstem. …"
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Is there any Genetic Correlation between CACNA1A Gene and Common Migraine in Iran? oleh Maryam Ostadsharif, Abbas Ghorbani, Mansoor Salehi, Rokhsareh Meamar

Subjek: "…Familial hemiplegic migraine (FHM)…"
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