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1

Hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome with evidence of mitochondrial dysfunction due to a novel SLC25A15 (ORNT1) gene mutation in a Palestinian family

Stanley H. Korman, Naomi Kanazawa, Bassam Abu-Libdeh, Alisa Gutman, Seiichi Tsujino

Journal:

Journal of the Neurological Sciences

Year:

2004

Language:

english

File:

PDF, 331 KB

english, 2004

2

Clinical Reasoning: A 17-year-old baseball player with right hand weakness

Vachon, Christopher, Abu Libdeh, Amal

Journal:

Year:

2019

Language:

english

File:

PDF, 310 KB

english, 2019

3

Autosomal recessive familial neurohypophyseal diabetes insipidus: onset in early infancy

Abu Libdeh, A., Levy-Khademi, F., Abdulhadi-Atwan, M., Bosin, E., Korner, M., White, P. C, Zangen, D. H

Journal:

European Journal of Endocrinology

Year:

2010

Language:

english

File:

PDF, 201 KB

english, 2010

4

Iatrogenic Cushing Syndrome due to Intranasal Dexamethasone

Rottenstreich, A., Wexler, I. D., Abu-Libdeh, A., Berkun, Y.

Journal:

Clinical Pediatrics

Year:

2014

Language:

english

File:

PDF, 280 KB

english, 2014

5

Syndrome of cleft palate, microcephaly, large ears, and short stature (Say syndrome)

Bassam Abu-Libdeh, Atsuko Fujimoto, Marcia Ehinger

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 758 KB

english, 1993

6

Tricho-hepato-enteric syndrome: A case of hemochromatosis with intractable diarrhea, dysmorphic features, and hair abnormality

Imad Dweikat, Mutaz Sultan, Nizar Maraqa, Tareq Hindi, Sara Abu-Rmeileh, Bassam Abu-Libdeh

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 108 KB

english, 2007

7

Relationship of Neurologic Degeneration to Genotype in Three Xeroderma Pigmentosum Group G Patients1

Emmert, Steffen, Slor, Hanoch, Busch, David B., Batko, Sima, Albert, Roberta B., Coleman, Donna, Khan, Sikandar G., Abu-Libdeh, Bassam, DiGiovanna, John J., Cunningham, Bari B., Lee, Myung-Moo, Crolli

Journal:

The Journal of Investigative Dermatology

Year:

2002

Language:

english

File:

PDF, 438 KB

english, 2002

8

Aspartylglucosaminuria among Palestinian Arabs

J. Zlotogora, Z. Ben-Neriah, B. Y. Abu-Libdeh, M. Zeigler

Journal:

Journal of Inherited Metabolic Disease

Year:

1997

Language:

english

File:

PDF, 26 KB

english, 1997

9

Dynamics of topological defects in a two-dimensional magnetic domain stripe pattern

Abu-Libdeh, N., Venus, D.

Journal:

Physical Review B

Year:

2011

Language:

english

File:

PDF, 360 KB

english, 2011

10

Further delineation of CANT1 phenotypic spectrum and demonstration of its role in proteoglycan synthesis

Mathilde Nizon, Céline Huber, Fabio De Leonardis, Rodolphe Merrina, Antonella Forlino, Mélanie Fradin, Beyhan Tuysuz, Bassam Y. Abu-Libdeh, Yasemin Alanay, Beate Albrecht, Lihadh Al-Gazali, Sarenur Yi

Journal:

Year:

2012

Language:

english

File:

PDF, 315 KB

english, 2012

11

A computer program for the statistical analysis of repeated event data using a mixed effects regression model

Ranjini Natarajan, Bruce W. Turnbull, Elizabeth H. Slate, Martin T. Wells, Larry C. Clark, Hasan Abu-Libdeh

Journal:

Computer Methods and Programs in Biomedicine

Year:

1994

Language:

english

File:

PDF, 598 KB

english, 1994

12

Initial susceptibility of iron in mercury magnetic fluids

I. Abu-Aljarayesh, A. Abu-Libdeh

Journal:

Journal of Magnetism and Magnetic Materials

Year:

1991

Language:

english

File:

PDF, 667 KB

english, 1991

13

The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3

Vered Molho-Pessach, Israela Lerer, Dvorah Abeliovich, Ziad Agha, Abdulasalam Abu Libdeh, Valentina Broshtilova, Orly Elpeleg, Abraham Zlotogorski

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 692 KB

english, 2008

14

XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription

David Zangen, Yotam Kaufman, Sharon Zeligson, Shira Perlberg, Hila Fridman, Moein Kanaan, Maha Abdulhadi-Atwan, Abdulsalam Abu Libdeh, Ayal Gussow, Irit Kisslov, Liran Carmel, Paul Renbaum, Ephrat Lev

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 720 KB

english, 2011

15

Propionic acidemia mimicking diabetic ketoacidosis

Imad M. Dweikat, Enas N. Naser, Abdulsalam I. Abu Libdeh, Osama J. Naser, Najwan N. Abu Gharbieh, Nizar F. Maraqa, Bassam Y. Abu Libdeh

Journal:

Brain and Development

Year:

2011

Language:

english

File:

PDF, 144 KB

english, 2011

16

When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patients

Ruth Bargal, Marsha Zeigler, Bassam Abu-Libdeh, Vivi Zuri, Hanna Mandel, Ziva Ben Neriah, Fiona Stewart, Nursel Elcioglu, Tareq Hindi, Martine Le Merrer, Gideon Bach, Annick Raas-Rothschild

Journal:

Molecular Genetics and Metabolism

Year:

2006

Language:

english

File:

PDF, 192 KB

english, 2006

17

Corrigendum to “When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patients” [Mol. Genet. Metab. 88 (2006) 359–363]

Ruth Bargal, Marsha Zeigler, Bassam Abu-Libdeh, Vivi Zuri, Hanna Mandel, Ziva Ben Neriah, Fiona Stewart, Nursel Elcioglu, Tareq Hindi, Martine Le Merrer, Gideon Bach, Annick Raas-Rothschild

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 77 KB

english, 2007

18

Interaction of Pulmonary Surfactant Protein SP-A with DPPC/Egg-PG Bilayers

Morrow, Michael R., Abu-Libdeh, Nidal, Stewart, June, Keough, Kevin M.W.

Journal:

Biophysical Journal

Year:

2003

Language:

english

File:

PDF, 167 KB

english, 2003

19

Ethylmalonic encephalopathy associated with crescentic glomerulonephritis

Dweikat, Imad, Naser, Enas, Damsah, Nadera, Libdeh, Bassam Abu, Bakri, Izzeddin

Journal:

Metabolic Brain Disease

Year:

2012

Language:

english

File:

PDF, 275 KB

english, 2012

20

Dynamics of domain growth driven by dipolar interactions in a perpendicularly magnetized ultrathin film

Abu-Libdeh, N., Venus, D.

Journal:

Physical Review B

Year:

2010

Language:

english

File:

PDF, 484 KB

english, 2010

21

[ACM Press the 1st ACM symposium - Indianapolis, Indiana, USA (2010.06.10-2010.06.11)] Proceedings of the 1st ACM symposium on Cloud computing - SoCC '10 - RACS

Abu-Libdeh, Hussam, Princehouse, Lonnie, Weatherspoon, Hakim

Year:

2010

Language:

english

File:

PDF, 489 KB

english, 2010

22

Epidemiological and Microbiological Characteristics of an Outbreak Caused by OXA-48-Producing Enterobacteriaceae in a Neonatal Intensive Care Unit in Jerusalem, Israel

Adler, A., Solter, E., Masarwa, S., Miller-Roll, T., Abu-Libdeh, B., Khammash, H., Najem, K., Dekadek, S., Stein-Zamir, C., Nubani, N., Kunbar, A., Assous, M. V., Carmeli, Y., Schwaber, M. J.

Journal:

Journal of Clinical Microbiology

Year:

2013

Language:

english

File:

PDF, 341 KB

english, 2013

23

The effects of topical and oral L‐selenomethionine on pigmentation and skin cancer induced by ultraviolet irradiation

Burke, Karen E., Combs, Gerald F., Gross, Earl G., Bhuyan, Kailash C., Abu‐Libdeh, Hassan

Journal:

Nutrition and Cancer

Year:

1992

Language:

english

File:

PDF, 1.00 MB

english, 1992

24

Dynamical signature of a domain phase transition in a perpendicularly magnetized ultrathin film

Abu-Libdeh, N., Venus, D.

Journal:

Physical Review B

Year:

2009

Language:

english

File:

PDF, 500 KB

english, 2009

25

Novel De Novo Mutation in Sulfonylurea Receptor 1 Presenting as Hyperinsulinism in Infancy Followed by Overt Diabetes in Early Adolescence

Abdulhadi-Atwan, M., Bushman, J. D., Tornovsky-Babaey, S., Perry, A., Abu-Libdeh, A., Glaser, B., Shyng, S.-L., Zangen, D. H.

Journal:

Year:

2008

Language:

english

File:

PDF, 299 KB

english, 2008

26

A defect in the retromer accessory protein, SNX27, manifests by infantile myoclonic epilepsy and neurodegeneration

Damseh, Nadirah, Danson, Chris M., Al-Ashhab, Motee, Abu-Libdeh, Bassam, Gallon, Matthew, Sharma, Kanchan, Yaacov, Barak, Coulthard, Elizabeth, Caldwell, Maeve A., Edvardson, Simon, Cullen, Peter J.,

Journal:

Year:

2015

Language:

english

File:

PDF, 732 KB

english, 2015

27

Familial Autosomal Recessive Renal Tubular Acidosis: Importance of Early Diagnosis

Vivante, Asaf, Lotan, Danny, Pode-Shakked, Naomi, Landau, Daniel, Svec, Peter, Nampoothiri, Sheela, Verma, Ishwar, Abu-Libdeh, Abdulsalam, Bockenhauer, Detlef, Dekel, Benjamin, Anikster, Yair

Journal:

Nephron Physiology

Year:

2011

Language:

english

File:

PDF, 607 KB

english, 2011

28

A syndrome including thumb malformations, microcephaly, short stature, and hypogonadism.

Zlotogora, J, Dagan, J, Ganen, A, Abu-Libdeh, M, Ben-Neriah, Z, Cohen, T

Journal:

Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 589 KB

english, 1997

29

A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions

Melchionda, Laura, Damseh, Nadirah S., Abu Libdeh, Bassam Y., Nasca, Alessia, Elpeleg, Orly, Zanolini, Alice, Ghezzi, Daniele

Journal:

Frontiers in Genetics

Year:

2014

Language:

english

File:

PDF, 1.35 MB

english, 2014

30

Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress

Weinberg-Shukron, A., Abu-Libdeh, A., Zhadeh, F., Carmel, L., Kogot-Levin, A., Kamal, L., Kanaan, M., Zeligson, S., Renbaum, P., Levy-Lahad, E., Zangen, D.

Journal:

Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 5.15 MB

english, 2015

31

[ACM Press the Twenty-Fourth ACM Symposium - Farminton, Pennsylvania (2013.11.03-2013.11.06)] Proceedings of the Twenty-Fourth ACM Symposium on Operating Systems Principles - SOSP '13 - Consistency-based service level agreements for cloud storage

Terry, Douglas B., Prabhakaran, Vijayan, Kotla, Ramakrishna, Balakrishnan, Mahesh, Aguilera, Marcos K., Abu-Libdeh, Hussam

Year:

2013

Language:

english

File:

PDF, 1.17 MB

english, 2013

32

[ACM Press the ACM SIGCOMM 2010 conference - New Delhi, India (2010.08.30-2010.09.03)] Proceedings of the ACM SIGCOMM 2010 conference on SIGCOMM - SIGCOMM '10 - Symbiotic routing in future data centers

Abu-Libdeh, Hussam, Costa, Paolo, Rowstron, Antony, O'Shea, Greg, Donnelly, Austin

Year:

2010

Language:

english

File:

PDF, 628 KB

english, 2010

33

Symbiotic routing in future data centers

Abu-Libdeh, Hussam, Costa, Paolo, Rowstron, Antony, O'Shea, Greg, Donnelly, Austin

Journal:

ACM SIGCOMM Computer Communication Review

Year:

2010

Language:

english

File:

PDF, 628 KB

english, 2010

34

[ACM Press the 4th annual Symposium - Santa Clara, California (2013.10.01-2013.10.03)] Proceedings of the 4th annual Symposium on Cloud Computing - SOCC '13 - Leveraging sharding in the design of scalable replication protocols

Abu-Libdeh, Hussam, van Renesse, Robbert, Vigfusson, Ymir

Year:

2013

Language:

english

File:

PDF, 301 KB

english, 2013

35

[ACM Press the 2nd Workshop - Yorktown Heights, New York (2008.09.15-2008.09.17)] Proceedings of the 2nd Workshop on Large-Scale Distributed Systems and Middleware - LADIS '08 - Dr. Multicast

Vigfusson, Ymir, Abu-Libdeh, Hussam, Balakrishnan, Mahesh, Birman, Ken, Tock, Yoav

Year:

2008

Language:

english

File:

PDF, 232 KB

english, 2008

36

[ACM Press the 5th European conference - Paris, France (2010.04.13-2010.04.16)] Proceedings of the 5th European conference on Computer systems - EuroSys '10 - Dr. multicast

Vigfusson, Ymir, Abu-Libdeh, Hussam, Balakrishnan, Mahesh, Birman, Ken, Burgess, Robert, Chockler, Gregory, Li, Haoyuan, Tock, Yoav

Year:

2010

Language:

english

File:

PDF, 612 KB

english, 2010

37

Analysis of Multi-Type Recurrent Events in Longitudinal Studies; Application to a Skin Cancer Prevention Trial

Hasan Abu-Libdeh, Bruce W. Turnbull and Larry C. Clark

Journal:

Year:

1990

Language:

english

File:

PDF, 2.05 MB

english, 1990

38

Arab League Educational, Cultural and Scientific Organization (ALECSO)

Libdeh, Asaad Abu, Harris, Brian

Journal:

Year:

1986

Language:

english

File:

PDF, 433 KB

english, 1986

39

Deleterious mutation in GPR88 is associated with chorea, speech delay, and learning disabilities

Alkufri, Fadi, Shaag, Avraham, Abu-Libdeh, Bassam, Elpeleg, Orly

Journal:

Neurology: Genetics

Year:

2016

Language:

english

File:

PDF, 356 KB

english, 2016

40

Teaching Neuro Images : Intracranial hypotension in a patient with Marfan syndrome

Abu Libdeh, Amal, Matsumoto, Julie A., Dhamija, Radhika

Journal:

Year:

2016

Language:

english

File:

PDF, 313 KB

english, 2016

41

GLP-1-RA corrects mitochondrial labile iron accumulation and improves β-cell function in type 2 Wolfram syndrome

Danielpur, Liron, Sohn, Yang-Sung, Karmi, Ola, Fogel, Chen, Zinger, Adar, Abu-Libdeh, Abdulsalam, Israeli, Tal, Riahi, Yael, Pappo, Orit, Birk, Ruth, Zangen, David H, Mittler, Ron, Cabantchik, Zvi-Ioa

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2016

Language:

english

File:

PDF, 2.29 MB

english, 2016

42

PARP10 deficiency manifests by severe developmental delay and DNA repair defect

Shahrour, Maher Awni, Nicolae, Claudia M., Edvardson, Simon, Ashhab, Motee, Galvan, Adri M., Constantin, Daniel, Abu-Libdeh, Bassam, Moldovan, George-Lucian, Elpeleg, Orly

Journal:

Year:

2016

Language:

english

File:

PDF, 2.03 MB

english, 2016

43

Acute Disseminated Encephalomyelitis: A Gray Distinction

Abu Libdeh, Amal, Goodkin, Howard P., Ramirez-Montealegre, Denia, Brenton, J. Nicholas

Journal:

Pediatric Neurology

Year:

2017

Language:

english

File:

PDF, 566 KB

english, 2017

44

Clinical heterogeneity of glycine encephalopathy in three Palestinian siblings: A novel mutation in the glycine decarboxylase ( GLDC ) gene

Khraim, Waseem, Abu-Libdeh, Bassam, Ayesh, Suhail, Dweikat, Imad

Journal:

Brain and Development

Year:

2017

Language:

english

File:

PDF, 680 KB

english, 2017

45

Clinical Reasoning: A 13-year-old boy with chronic ataxia and developmental delay

Abu Libdeh, Amal, Talman, Lauren, Chambers, Chelsea, Dhamija, Radhika

Journal:

Year:

2017

Language:

english

File:

PDF, 277 KB

english, 2017

46

Mutations in the phosphatidylinositol glycan C ( PIGC ) gene are associated with epilepsy and intellectual disability

Edvardson, Simon, Murakami, Yoshiko, Nguyen, Thi Tuyet Mai, Shahrour, Maher, St-Denis, Anik, Shaag, Avraham, Damseh, Nadira, Le Deist, Françoise, Bryceson, Yenan, Abu-Libdeh, Bassam, Campeau, Philippe

Journal:

Journal of Medical Genetics

Year:

2017

Language:

english

File:

PDF, 1.17 MB

english, 2017

47

Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation

Molho-Pessach, Vered, Ramot, Yuval, Mogilevsky, Maxim, Cohen-Daniel, Leonor, Eisenstein, Eli M., Abu-Libdeh, Abdulsalam, Siam, Ihab, Berger, Michael, Karni, Rotem, Zlotogorski, Abraham

Journal:

Journal of Dermatological Science

Year:

2017

Language:

english

File:

PDF, 1.27 MB

english, 2017

48

Hypomyelinating leukodystrophy associated with a deleterious mutation in the ATRN gene

Shahrour, Maher Awni, Ashhab, Motee, Edvardson, Simon, Gur, Michal, Abu-Libdeh, Bassam, Elpeleg, Orly

Journal:

Year:

2017

Language:

english

File:

PDF, 1.54 MB

english, 2017

49

A Novel Mutation in the AVPR2 Gene in a Palestinian Family with Nephrogenic Diabetes Insipidus

Abu-Libdeh, Abdulsalam, Wexler, Isaiah, Dweikat, Imad, Zangen, David, Abu-Libdeh, Bassam

Journal:

Journal of Child Science

Year:

2017

Language:

english

File:

PDF, 857 KB

english, 2017

50

A Novel Mutation in the CLDN16 Gene in a Palestinian Family with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

Abu-Libdeh, Abdulsalam, Abu-Libdeh, Bassam, Abdulhag, Ulla

Journal:

Journal of Child Science

Year:

2017

Language:

english

File:

PDF, 174 KB

english, 2017