Mahajnah, M.: search on Z-Library

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1

Cognition, psychosocial adjustment and coping in familial cases of velocardiofacial syndrome

D. Gothelf, A. Aviram-Goldring, M. Burg, T. Steinberg, M. Mahajnah, A. Frisch, S. Fennig, G. Zalsman, A. Weizman

Journal:

Journal of Neural Transmission

Year:

2007

Language:

english

File:

PDF, 110 KB

english, 2007

2

First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery

Hengel, Holger, Buchert, Rebecca, Sturm, Marc, Haack, Tobias B., Schelling, Yvonne, Mahajnah, Muhammad, Sharkia, Rajech, Azem, Abdussalam, Balousha, Ghassan, Ghanem, Zaid, Falana, Mohammed, Balousha,

Journal:

European Journal of Human Genetics

Year:

2020

Language:

english

File:

PDF, 852 KB

english, 2020

3

The Influence of Excessive Chewing Gum Use on Headache Frequency and Severity Among Adolescents

Watemberg, Nathan, Matar, Manar, Har-Gil, Miki, Mahajnah, Muhammad

Journal:

Pediatric Neurology

Year:

2014

Language:

english

File:

PDF, 170 KB

english, 2014

4

Pseudotumor Cerebri Syndrome in Young Children: What Is the Difference From Adults?

Genizi, Jacob, Mahajnah, Muhammad

Journal:

Journal of Child Neurology

Year:

2020

File:

PDF, 90 KB

2020

5

Pediatric-Onset Gelastic Seizures: Clinical Data and Outcome

Eli Shahar, Uri Kramer, Muhammad Mahajnah, Tallie Lerman-Sagie, Rachel Goez, Varda Gross, Miriam Kutai, Jacob Genizi

Journal:

Pediatric Neurology

Year:

2007

Language:

english

File:

PDF, 88 KB

english, 2007

6

The Clinical Characteristics of ADHD Diagnosed in Adolescents in Comparison With Younger Children

Mahajnah, Muhammad, Sharkia, Rajech, Shorbaji, Nadeem, Zelnik, Nathanel

Journal:

Journal of Attention Disorders

Year:

2017

Language:

english

File:

PDF, 301 KB

english, 2017

7

A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal Microcephaly

Ganeshwaran H. Mochida, Muhammad Mahajnah, Anthony D. Hill, Lina Basel-Vanagaite, Danielle Gleason, R. Sean Hill, Adria Bodell, Moira Crosier, Rachel Straussberg, Christopher A. Walsh

Journal:

The American Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 1.01 MB

english, 2009

8

The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation

Mallaret, M., Synofzik, M., Lee, J., Sagum, C. A., Mahajnah, M., Sharkia, R., Drouot, N., Renaud, M., Klein, F. A. C., Anheim, M., Tranchant, C., Mignot, C., Mandel, J.-L., Bedford, M., Bauer, P., Sal

Journal:

Year:

2014

Language:

english

File:

PDF, 1.12 MB

english, 2014

9

Prevalence of epilepsy in Bedouin children: A cross-sectional study in Southern Israel

Zaid, Afawi, Abu-Hammad, Talab, Shorer, Zamir, Grotto, Itamar, Mahajnah, Muhammad

Journal:

Journal of Pediatric Neurology

Year:

2015

Language:

english

File:

PDF, 34 KB

english, 2015

10

Longiside, a Novel Digalactosylceramide from the Caribbean Sponge Agelas longissima

Francesco Cafieri, Ernesto Fattorusso, Yosef Mahajnah, Alfonso Mangoni

Journal:

European Journal of Organic Chemistry

Year:

1994

Language:

english

File:

PDF, 308 KB

english, 1994

11

Epidemiological characteristics of febrile seizures—Comparing between Bedouin and Jews in the Southern part of Israel

Avi Shimony, Zaid Afawi, Tal Asher, Muhammad Mahajnah, Zamir Shorer

Journal:

Year:

2009

Language:

english

File:

PDF, 185 KB

english, 2009

12

Phenotypic Heterogeneity in Consanguineous Patients With a Common CLN8 Mutation

Muhammad Mahajnah, Nathanel Zelnik

Journal:

Pediatric Neurology

Year:

2012

Language:

english

File:

PDF, 141 KB

english, 2012

13

Mental retardation and consanguinity in a selected region of the Israeli Arab community

Rajach Sharkia, Abdussalam Azem, Qassem Kaiyal, Nathanel Zelnik, Muhammad Mahajnah

Journal:

Central European Journal of Medicine

Year:

2010

Language:

english

File:

PDF, 1.18 MB

english, 2010

14

An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures

Straussberg, R., Basel-Vanagaite, L., Kivity, S., Dabby, R., Cirak, S., Nurnberg, P., Voit, T., Mahajnah, M., Inbar, D., Saifi, G. M.

Journal:

Year:

2005

Language:

english

File:

PDF, 147 KB

english, 2005

15

Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine

Kurolap, Alina, Armbruster, Anja, Hershkovitz, Tova, Hauf, Katharina, Mory, Adi, Paperna, Tamar, Hannappel, Ewald, Tal, Galit, Nijem, Yusif, Sella, Ella, Mahajnah, Muhammad, Ilivitzki, Anat, Hershkovi

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.07 MB

english, 2016

16

Familial Cognitive Impairment With Ataxia With Oculomotor Apraxia

Mahajnah, M., Basel-Vanagaite, L., Inbar, D., Kornreich, L., Weitz, R., Straussberg, R.

Journal:

Journal of Child Neurology

Year:

2005

Language:

english

File:

PDF, 418 KB

english, 2005

17

Multiplex families with epilepsy: Success of clinical and molecular genetic characterization

Afawi, Z., Oliver, K. L., Kivity, S., Mazarib, A., Blatt, I., Neufeld, M. Y., Helbig, K. L., Goldberg-Stern, H., Misk, A. J., Straussberg, R., Walid, S., Mahajnah, M., Lerman-Sagie, T., Ben-Zeev, B.,

Journal:

Year:

2016

Language:

english

File:

PDF, 654 KB

english, 2016

18

Parental mosaicism in another case of Dravet syndrome caused by a novel SCN1A deletion: a case report

Sharkia, Rajech, Hengel, Holger, Schöls, Ludger, Athamna, Muhammad, Bauer, Peter, Mahajnah, Muhammad

Journal:

Journal of Medical Case Reports

Year:

2016

Language:

english

File:

PDF, 848 KB

english, 2016

19

A novel variant of the human mitochondrial DnaJ protein, Tid1, associates with a human disease exhibiting developmental delay and polyneuropathy

Patra, Malay, Weiss, Celeste, Abu-Libdeh, Bassam, Ashhab, Motee, Abuzer, Shadi, Elpeleg, Orly, Mahajnah, Muhammad, Kessel, Amit, Azem, Abdussalam

Journal:

European Journal of Human Genetics

Year:

2019

Language:

english

File:

PDF, 1.51 MB

english, 2019

20

Unraveling the genetic cause of hereditary ophthalmic disorders in Arab societies from Israel and the Palestinian Authority

Mayer, Anja K., Balousha, Ghassan, Sharkia, Rajech, Mahajnah, Muhammad, Ayesh, Suhail, Schulze, Martin, Buchert, Rebecca, Zobor, Ditta, Azem, Abdussalam, Schöls, Ludger, Bauer, Peter, Wissinger, Bernd

Journal:

European Journal of Human Genetics

Year:

2020

File:

PDF, 1.30 MB

2020

21

P173 – 2561: The clinical profile of ADHD in Israel – Impact of ethnic and social diversities

Mahajnah, M., Sharkia, R., Shorbaji, N., Terkel-Dawer, R., Zelnik, N.

Journal:

European Journal of Paediatric Neurology

Year:

2015

Language:

english

File:

PDF, 92 KB

english, 2015

22

Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus

Mayer, Anja K, Mahajnah, Muhammad, Thomas, Mervyn G, Cohen, Yuval, Habib, Adib, Schulze, Martin, Maconachie, Gail D E, AlMoallem, Basamat, De Baere, Elfride, Lorenz, Birgit, Traboulsi, Elias I, Kohl,

Journal:

Year:

2019

Language:

english

File:

PDF, 510 KB

english, 2019

23

Sanfilippo type A: new clinical manifestations and neuro-imaging findings in patients from the same family in Israel: a case report

Sharkia, Rajech, Mahajnah, Muhammad, Zalan, Abdelnaser, Sourlis, Chrysovalantis, Bauer, Peter, Schöls, Ludger

Journal:

Journal of Medical Case Reports

Year:

2014

Language:

english

File:

PDF, 295 KB

english, 2014

24

Clinical Characteristics of Autism Spectrum Disorder in Israel: Impact of Ethnic and Social Diversities

Mahajnah, Muhammad, Sharkia, Rajech, Shalabe, Haitham, Terkel-Dawer, Ruth, Akawi, Ashraf, Zelnik, Nathanel

Journal:

BioMed Research International

Year:

2015

Language:

english

File:

PDF, 1.21 MB

english, 2015

25

Comparative screening of FMF mutations in various communities of the Israeli society

Sharkia, Rajech, Mahajnah, Muhammad, Zalan, Abdelnaser, Athamna, Muhammad, Azem, Abdussalam, Badarneh, Khader, Faris, Fuad

Journal:

European Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 246 KB

english, 2013

26

Familial Cognitive Impairment With Ataxia With Oculomotor Apraxia

Mahajnah, M., Basel-Vanagaite, L., Inbar, D., Kornreich, L., Weitz, R., Straussberg, R.

Journal:

Journal of Child Neurology

Year:

2005

Language:

english

File:

PDF, 162 KB

english, 2005

27

The impact of nutritional vitamin B12, folate and hemoglobin deficiency on school performance of elementary school children

R. Masalha, Z. Afawi, M. Mahajnah, A. Mashal, M. Hallak, I. Alsaied, A. Bolotin, G. Ifergan, I. Wirguin

Year:

2015

Language:

english

File:

PDF, 46 KB

english, 2015

28

CHANGES IN MARRIAGE PATTERNS AMONG THE ARAB COMMUNITY IN ISRAEL OVER A 60-YEAR PERIOD

Sharkia, Rajech, Mahajnah, Muhammad, Athamny, Esmael, Khatib, Mohammad, Sheikh-Muhammad, Ahmad, Zalan, Abdelnaser

Journal:

Journal of Biosocial Science

Year:

2016

Language:

english

File:

PDF, 68 KB

english, 2016

29

Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus

Mayer, Anja K, Mahajnah, Muhammad, Thomas, Mervyn G, Cohen, Yuval, Habib, Adib, Schulze, Martin, Maconachie, Gail D E, AlMoallem, Basamat, De Baere, Elfride, Lorenz, Birgit, Traboulsi, Elias I, Kohl,

Journal:

Year:

2019

File:

PDF, 510 KB

2019

30

A new case confirming and expanding the phenotype spectrum of ADAT3-related intellectual disability syndrome

Sharkia, Rajech, Zalan, Abdelnaser, Jabareen-Masri, Azhar, Zahalka, Hazar, Mahajnah, Muhammad

Journal:

European Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 653 KB

english, 2018

31

Clinical features at the time of diagnosis of benign epilepsy with centrotemporal spikes do not predict subsequent seizures

Watemberg, Nathan, Afunevitz, Sveta, Ganelin-Cohen, Esther, Mahajnah, Muhammad

Journal:

Pediatric Neurology

Year:

2018

Language:

english

File:

PDF, 411 KB

english, 2018

32

6-Bromo-5-hydroxy-3-indolecarboxyaldehyde from the Caribbean sponge Oceanapia bartschi

Cafieri, Francesco, Fattorusso, Ernesto, Mahajnah, Yosef, Mangoni, Alfonso

Journal:

Zeitschrift für Naturforschung B

Year:

1993

Language:

english

File:

PDF, 2.77 MB

english, 1993

33

Microvillous Inclusion Disease: Ultrastructural Variability

Iancu, Theodore C., Mahajnah, Muhammad, Manov, Irena, Shaoul, Ron

Journal:

Ultrastructural Pathology

Year:

2007

Language:

english

File:

PDF, 6.43 MB

english, 2007

34

A novel variant of the human mitochondrial DnaJ protein, Tid1, associates with a human disease exhibiting developmental delay and polyneuropathy

Patra, Malay, Weiss, Celeste, Abu-Libdeh, Bassam, Ashhab, Motee, Abuzer, Shadi, Elpeleg, Orly, Mahajnah, Muhammad, Kessel, Amit, Azem, Abdussalam

Journal:

European Journal of Human Genetics

Year:

2019

File:

PDF, 1.51 MB

2019

35

A novel biallelic loss‐of‐function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro‐facio‐thoracic dysplasia

Sharkia, Rajech, Zalan, Abdelnaser, Jabareen‐Masri, Azhar, Hengel, Holger, Schöls, Ludger, Kessel, Amit, Azem, Abdussalam, Mahajnah, Muhammad

Journal:

American Journal of Medical Genetics Part A

Year:

2019

Language:

english

File:

PDF, 1.19 MB

english, 2019

36

Childhood-Onset Idiopathic Intracranial Hypertension: Relation of Sex and Obesity

Jacob Genizi, Eli Lahat, Nathanel Zelnik, Muhammad Mahajnah, Sarit Ravid, Eli Shahar

Journal:

Pediatric Neurology

Year:

2007

Language:

english

File:

PDF, 72 KB

english, 2007

37

Alexander Disease in Israel: Megalencephaly and Leukoencephalopathy and Its Differential Diagnosis

Mahajnah, Muhammad, Abu-Rashid, Muhammad, Lerman-Sagie, Tally, Goikhman, Igor, Zelnik, Nathanel

Journal:

Journal of Pediatric Neurology

Year:

2015

Language:

english

File:

PDF, 117 KB

english, 2015

38

Case 1: Seizures and Rashes Do Run in the Family

Hochberg, Amit, Foldi, Sylvia, Nadir, Erez, Shreter, Roni, Mahajnah, Muhammad, Feldman, Michael

Journal:

Year:

2017

Language:

english

File:

PDF, 1.16 MB

english, 2017

39

A prospective case study of the safety and efficacy of lysine restricted diet and arginine supplementation therapy in a patient with pyridoxine-dependent epilepsy caused by mutations in ALDH7A1

Mahajnah, Muhammad, Corderio, Dawn, Austin, Valerie, Herd, Sarah, Mutch, Carly, Carter, Melissa, Struys, Eduard, Mercimek-Mahmutoglu, Saadet

Journal:

Pediatric Neurology

Year:

2016

Language:

english

File:

PDF, 327 KB

english, 2016

40

Benign Hereditary Chorea: Clinical, Neuroimaging, and Genetic Findings

Mahajnah, M., Inbar, D., Steinmetz, A., Heutink, P., Breedveld, G.J., Straussberg, R.

Journal:

Journal of Child Neurology

Year:

2007

Language:

english

File:

PDF, 1.24 MB

english, 2007

41

The clinical characteristics of attention deficit hyperactivity

Mahajnah, M., Zelnik, N.

Journal:

European Journal of Paediatric Neurology

Year:

2017

Language:

english

File:

PDF, 42 KB

english, 2017

42

Gene and Protein Expression in Subjects With a Nystagmus-Associated AHR Mutation

Borovok, Natalia, Weiss, Celeste, Sharkia, Rajech, Reichenstein, Michal, Wissinger, Bernd, Azem, Abdussalam, Mahajnah, Muhammad

Journal:

Frontiers in Genetics

Year:

2020

File:

PDF, 1.22 MB

2020

43

Corrigendum to âAbsence seizure provocation during routine EEG: Does position of the child during hyperventilation affect diagnostic yield?â [Seizure 79 (2020) 86â89]

Rozenblat, Tal, Kraus, Dror, Mahajnah, Muhammad, Goldberg-Stern, Hadassah, Watemberg, Nathan

Journal:

Year:

2020

File:

PDF, 1.15 MB

2020

44

Complete 1H and 13C NMR assignment of ent-3β,16α-atisanediol, a cytotoxic diterpene isolated from the sponge Spirastrella cunctatrix

Francesco Cafieri, Ernesto Fattorusso, Yosef Mahajnah, Alfonso Mangoni

Journal:

Magnetic Resonance in Chemistry

Year:

1995

Language:

english

File:

PDF, 392 KB

english, 1995

45

A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab–Israeli family

Abu-Rashid, M., Mahajnah, M., Jaber, L., Kornreich, L., Bar-On, E., Basel-Vanagaite, L., Soffer, D., Koenig, M., Straussberg, R.

Journal:

European Journal of Paediatric Neurology

Year:

2013

Language:

english

File:

PDF, 888 KB

english, 2013

46

The Liver in Congenital Disorders of Glycosylation: Ultrastructural Features

Iancu, Theodore C., Mahajnah, Muhammad, Manov, Irena, Cherurg, Sigal, Knopf, Carlos, Mandel, Hanna

Journal:

Ultrastructural Pathology

Year:

2007

Language:

english

File:

PDF, 5.09 MB

english, 2007

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