FRYDMAN, MOSHE: search on Z-Library

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1

Citrus fruit flavor and aroma biosynthesis: isolation, functional characterization, and developmental regulation of Cstps1, a key gene in the production of the sesquiterpene aroma compound valencene

Liat Sharon-Asa, Moshe Shalit, Ahuva Frydman, Einat Bar, Doron Holland, Etti Or, Uri Lavi, Efraim Lewinsohn, Yoram Eyal

Journal:

The Plant Journal

Year:

2003

Language:

english

File:

PDF, 151 KB

english, 2003

2

Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

Doron Gothelf, Gadi Presburger, Ada H. Zohar, Merav Burg, Ariela Nahmani, Moshe Frydman, Mordechai Shohat, Dov Inbar, Ayala Aviram-Goldring, Josepha Yeshaya, Tamar Steinberg, Yehuda Finkelstein, Amos

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2004

Language:

english

File:

PDF, 81 KB

english, 2004

3

Noonan syndrome: A cryptic condition in early gestation

Achiron, Reuwen, Heggesh, J., Grisaru, Dan, Goldman, Boleslav, Lipitz, Shlomo, Yagel, Simcha, Frydman, Moshe

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 313 KB

english, 2000

4

Familial Syndromic Esophageal Atresia Maps to 2p23-p24

Jacopo Celli, Ellen van Beusekom, Raoul C.M. Hennekam, M. Esther Gallardo, Dominique F.C.M. Smeets, Santiago Rodríguez de Córdoba, Jeffrey W. Innis, Moshe Frydman, Rainer König, Helen Kingston, John T

Journal:

The American Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 1.03 MB

english, 2000

5

Familial lipoid adrenal hyperplasia: Genetic marker data and an approach to prenatal diagnosis

Dr. Moshe Frydman, Arieh Kauschansky, Rina Zamir, Batsheva Bonné-Tamir, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 623 KB

english, 1986

6

Familial segregation of cervical ribs, sprengel anomaly, preaxial polydactyly, anal atresia, and urethral obstruction: A new syndrome?

Dr. Moshe Frydman, Herman A. Cohen, Arie Ashkenazi, Itzhak Varsano

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 610 KB

english, 1993

7

Add-on prolonged-release melatonin for cognitive function and sleep in mild to moderate Alzheimer’s disease: a 6-month, randomized, placebo-controlled, multicenter trial

Laudon, Moshe, G Wade, Alan, Farmer, Mildred, Harari, Gil, Fund, Naama, Nir, Tali, Frydman-Marom, Anat, Zisapel, Nava

Journal:

Clinical Interventions in Aging

Year:

2014

Language:

english

File:

PDF, 909 KB

english, 2014

8

PRENATAL DIAGNOSIS OF RAMBAM–HASHARON SYNDROME

MOSHE FRYDMAN, DAVID VARDIMON, ELIEZER SHALEV, JEROME B. ORLIN

Journal:

Prenatal Diagnosis

Year:

1996

Language:

english

File:

PDF, 341 KB

english, 1996

9

No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome

Rachel Pesso, G. Barkai, Yehoshua Ravia, E. Gak, Moshe Frydman, Boleslaw Goldman, E. Friedman

Journal:

Year:

1997

Language:

english

File:

PDF, 31 KB

english, 1997

10

Molecular cytogenetic studies in three patients with partial trisomy 2p, including CGH from paraffin-embedded tissue

Aviram-Goldring, Ayala, Fritz, Barbara, Bartsch, Christine, Steuber, Elke, Daniely, Michal, Lev, Dorit, Chaki, Rina, Barkai, Gad, Frydman, Moshe, Rehder, Helga

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 698 KB

english, 2000

11

Chromosome abnormalities in infants with prune belly anomaly: Association with trisomy 18

Moshe Frydman, R. Ellen Magenis, T. K. Mohandas, Dr. Michael M. Kaback, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1983

Language:

english

File:

PDF, 244 KB

english, 1983

12

Erratum: Genetic and biochemical analyses of Israeli osteogenesis imperfecta patients

Liat Ries-Levavi, Tsofia Ish-Shalom, Moshe Frydman, Dorit Lev, Shirley Cohen, Gad Barkai, Boleslaw Goldman, Peter Byers, Eitan Friedman

Journal:

Year:

2004

Language:

english

File:

PDF, 16 KB

english, 2004

13

Historical note: an analysis of a 17th century illustration of a child with split hand/split foot malformation

Avi Ohry, Moshe Frydman

Journal:

Journal of Children's Orthopaedics

Year:

2010

Language:

english

File:

PDF, 129 KB

english, 2010

14

A single origin of phenylketonuria in Yemenite Jews

Avigad, Smadar, Cohen, Bernard E., Bauer, Sofia, Schwartz, Gerard, Frydman, Moshe, Woo, Savio L. C., Niny, Yehuda, Shiloh, Yosef

Journal:

Year:

1990

File:

PDF, 501 KB

1990

15

The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22–q23

Ziv, Yael, Rotman, Galit, Frydman, Moshe, Dagan, Judith, Cohen, Tirza, Foroud, Tatiana, Gatti, Richard A., Shiloh, Yosef

Journal:

Year:

1991

Language:

english

File:

PDF, 251 KB

english, 1991

16

Hyperprolactinemia after treatment of long-acting gonadotropin-releasing hormone analogue Decapeptyl* in girls with central precocious puberty*Decapeptyl, D-Trp6, Ferring, Malmo, Sweden.

Kauschansky, Arieh, Nussinovitch, Moshe, Frydman, Moshe, Yeshaya, Arie, Ben-Rafael, Zion

Journal:

Fertility and Sterility

Year:

1995

Language:

english

File:

PDF, 335 KB

english, 1995

17

Single Intramuscular Dose of Ceftriaxone as Compared to 7-Day Amoxicillin Therapy for Acute Otitis Media in Children

Varsano, Izhak, Frydman, Moshe, Amir, Jacob, Alpert, Gershon

Journal:

Year:

1988

File:

PDF, 2.23 MB

1988

18

Possible heterogeneity in spondyloenchondrodysplasia: Quadriparesis, basal ganglia calcifications, and chondrocyte inclusions

Moshe Frydman, Jacob Bar-Ziv, Rivka Preminger-Shapiro, Amichai Brezner, Natan Brand, Tamar Ben-Ami, Ralph S. Lachman, Helen E. Gruber, David L. Rimoin

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 692 KB

english, 1990

19

G2chromosomal radiosensitivity in families with ataxia-telangiectasia

Yosef Shiloh, Ram Parshad, Moshe Frydman, Katherine K. Sanford, Sima Portnoi, Yael Ziv, Gary M. Jones

Journal:

Year:

1989

Language:

english

File:

PDF, 438 KB

english, 1989

20

Benign paroxysmal torticollis in infancy

Cohen, Herman A., Nussinovitch, Moshe, Ashkenasi, Arie, Straussberg, Rachel, Kauschanksy, Arieh, Frydman, Moshe

Journal:

Pediatric Neurology

Year:

1993

Language:

english

File:

PDF, 279 KB

english, 1993

21

Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews

Bruria Ben-Zeev, Etgar Levy-Nissenbaum, Hadas Lahat, Yair Anikster, Yael Shinar, Nathan Brand, Varda Gross-Tzur, Daune MacGregor, Roy Sidi, Robert Kleta, Moshe Frydman, Elon Pras

Journal:

Year:

2002

Language:

english

File:

PDF, 96 KB

english, 2002

22

Genetic aspects of Wilson's disease

Journal:

Journal of Gastroenterology and Hepatology

Year:

1990

Language:

english

File:

PDF, 543 KB

english, 1990

23

Endocrine studies of the ovulatory disturbances in Wilson’s disease (hepatolenticular degeneration)

Kaushansky, Arieh, Frydman, Moshe, Kaufman, Hayuta, Homburg, Roy

Journal:

Fertility and Sterility

Year:

1987

Language:

english

File:

PDF, 512 KB

english, 1987

24

Leukonychia totalis in two sibs

Dr. Moshe Frydman, Hermann A. Cohen

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 154 KB

english, 1993

25

Oligodontia, short stature and small head circumference with normal intelligence

Yair Melamed, Mariasa Bat-Miriam Katznelson, Moshe Frydman

Journal:

Clinical Genetics

Year:

1994

Language:

english

File:

PDF, 225 KB

english, 1994

26

Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome

Doron Gothelf, Amos Frisch, Hanan Munitz, Rivka Rockah, Neil Laufer, Tamar Mozes, Haggai Hermesh, Abraham Weizman, Moshe Frydman

Journal:

Schizophrenia Research

Year:

1999

Language:

english

File:

PDF, 155 KB

english, 1999

27

Therapeutic Effects of Melatonin Receptor Agonists on Sleep and Comorbid Disorders

Laudon, Moshe, Frydman-Marom, Anat

Journal:

International Journal of Molecular Sciences

Year:

2014

Language:

english

File:

PDF, 722 KB

english, 2014

28

A Nonsense Mutation in the Glucosaminyl ( N -acetyl) Transferase 2 Gene ( GCNT2 ): Association with Autosomal Recessive Congenital Cataracts

Pras, Eran, Raz, Judith, Yahalom, Vered, Frydman, Moshe, Garzozi, Hanna J., Pras, Elon, Hejtmancik, J. Fielding

Journal:

Investigative Ophthalmology & Visual Science

Year:

2004

Language:

english

File:

PDF, 258 KB

english, 2004

29

Screening for fragile X syndrome in women of reproductive age

Rachel Pesso, Michal Berkenstadt, Howard Cuckle, Eva Gak, Lea Peleg, Moshe Frydman, Gad Barkai

Journal:

Prenatal Diagnosis

Year:

2000

Language:

english

File:

PDF, 59 KB

english, 2000

30

A Missense Mutation in the LIM2 Gene Is Associated with Autosomal Recessive Presenile Cataract in an Inbred Iraqi Jewish Family

Eran Pras, Etgar Levy-Nissenbaum, Tangiz Bakhan, Hadas Lahat, Ehud Assia, Noa Geffen-Carmi, Moshe Frydman, Boleslaw Goldman, Elon Pras

Journal:

The American Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 406 KB

english, 2002

31

Familial Lipoid Adrenal Hyperplasia

FRYDMAN, MOSHE, KAUSCHANSKY, ARIEH, ZAMIR, RINA, BONNÉ-TAMIR, BATSHEVA

Journal:

Obstetric and Gynecologic Survey

Year:

1987

File:

PDF, 2.12 MB

1987

32

Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in Israel

Shlomit Gilad, Rami Khosravi, Reli Harnik, Yael Ziv, Dganit Shkedy, Yaron Galanty, Moshe Frydman, Jacov Levi, Ozden Sanal, Luciana Chessa, Dominique Smeets, Yosef Shiloh, Anat Bar-Shira

Journal:

Year:

1998

Language:

english

File:

PDF, 196 KB

english, 1998

33

Assessment of the Hypothalamic-Pituitary-Testicular Function in Male Patients with Wilson's Disease

Dr. MOSHE FRYDMAN, ARIEH KAUSCHANSKY, BATSHEVA BONNE-TAMIR, FARES NASSAR, ROY HOMBURG

Journal:

Journal of Andrology

Year:

1991

Language:

english

File:

PDF, 698 KB

english, 1991

34

Connexin-Associated Deafness and Speech Perception Outcome of Cochlear Implantation

Taitelbaum-Swead, Riki, Brownstein, Zippora, Muchnik, Chava, Kishon-Rabin, Liat, Kronenberg, Jona, Megirov, Lela, Frydman, Moshe, Hildesheimer, Minka, Avraham, Karen B.

Journal:

Archives of Otolaryngology - Head and Neck Surgery

Year:

2006

Language:

english

File:

PDF, 115 KB

english, 2006

35

MODED: Microcephaly-oculo-digito-esophageal-duodenal syndrome

Frydman, Moshe, Katz, Miriam, Cabot, Susan G., Soen, Galia, Kauschansky, Arie, Sirota, Lea

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 1.08 MB

english, 1997

36

Familial simple hypohidrosis with abnormal palmar dermal ridges

Dr. Moshe Frydman, Herman A. Cohen, Arieh Kauschansky, Yehuda Matoth, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 427 KB

english, 1988

37

Neurologic Presentation in Children with Ataxia-Telangiectasia: Is Small Head Circumference a Hallmark of the Disease?

Andreea Nissenkorn, Yonit Banet Levi, Daphna Vilozni, Yakov Berkun, Ori Efrati, Moshe Frydman, Jacob Yahav, Dalia Waldman, Raz Somech, Efrat Shenhod, Shay Menascu, Bruria Ben-Zeev

Journal:

The Journal of Pediatrics

Year:

2011

Language:

english

File:

PDF, 471 KB

english, 2011

38

Deleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome

Almogit Abu, Moshe Frydman, Dina Marek, Eran Pras, Uri Nir, Haike Reznik-Wolf, Elon Pras

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 701 KB

english, 2008

39

Familial Lipoid Adrenal Hyperplasia

FRYDMAN, MOSHE, KAUSCHANSKY, ARIEH, ZAMIR, RINA, BONNÉ-TAMIR, BATSHEVA

Journal:

Obstetric and Gynecologic Survey

Year:

1987

File:

PDF, 2.12 MB

1987

40

Rambam–Hasharon syndrome of psychomotor retardation, short stature, defective neutrophil motility, and bombay phenotype

Dr. Moshe Frydman, Amos Etzioni, Tal Eidlitz-Markus, Israela Avidor, Itzhak Varsano, Yael Shechter, Jerome B. Orlin, Ruth Gershoni-Baruch

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 585 KB

english, 1992

41

X inactivation testing for identifying a non-syndromic X-linked mental retardation gene

Hagith Yonath, Dina Marek-Yagel, Haike Resnik-Wolf, Almogit Abu-Horvitz, Hagit N. Baris, Mordechai Shohat, Moshe Frydman, Elon Pras

Journal:

Journal of Applied Genetics

Year:

2011

Language:

english

File:

PDF, 142 KB

english, 2011

42

Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders

Nagamani, Sandesh C S, Erez, Ayelet, Ben-Zeev, Bruria, Frydman, Moshe, Winter, Susan, Zeller, Robert, El-Khechen, Dima, Escobar, Luis, Stankiewicz, Pawel, Patel, Ankita, Wai Cheung, Sau

Journal:

European Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 295 KB

english, 2013

43

Recurrent Severe Infections Caused by a Novel Leukocyte Adhesion Deficiency

Etzioni, Amos, Frydman, Moshe, Pollack, Shimon, Avidor, Israeli, Phillips, M. Laurie, Paulson, James C., Gershoni-Baruch, Ruth

Journal:

Boston Medical and Surgical Journal

Year:

1992

File:

PDF, 655 KB

1992

44

Reply to Drs. Rose and Bankier: OFD VI and C syndromes

Roxana Cleper, Arieh Kavschansky, Itzhak Varsano, Moshe Frydman

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 125 KB

english, 1994

45

Autosomal-dominant cutis laxa resulting from an intronic mutation in ELN

Vodo, Dan, Sarig, Ofer, Peled, Alon, Frydman, Moshe, Greenberger, Shoshi, Sprecher, Eli

Journal:

Experimental Dermatology

Year:

2015

Language:

english

File:

PDF, 445 KB

english, 2015

46

Prenatal diagnosis of nail-patella syndrome

Iain McIntosh, Mark V. Clough, Eva Gak, Moshe Frydman

Journal:

Prenatal Diagnosis

Year:

1999

Language:

english

File:

PDF, 116 KB

english, 1999

47

Váradi syndrome (OFD VI) or opitz trigonocephaly syndrome: Overlapping manifestations in two cousins

Roxana Cleper, Arieh Kaushchansky, Itzbak Varsano, Moshe Frydman

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 523 KB

english, 1993

48

Urodynamic Manifestations Associated with Ramsay-Hunt Syndrome

Cohen, Herman A., Abarbanel, Joseph, Ashkenasi, Arie, Frydman, Moshe, Straussberg, Rachel, Varsano, Itzhak

Journal:

Scandinavian Journal of Urology and Nephrology

Year:

1993

Language:

english

File:

PDF, 318 KB

english, 1993

49

Mapping of a Gene Causing Brittle Cornea Syndrome in Tunisian Jews to 16q24

Abu, Almogit, Frydman, Moshe, Marek, Dina, Pras, Eran, Stolovitch, Chaim, Aviram-Goldring, Ayala, Rienstein, Shlomit, Reznik-Wolf, Haike, Pras, Elon

Journal:

Investigative Ophthalmology & Visual Science

Year:

2006

Language:

english

File:

PDF, 181 KB

english, 2006

50

Interstitial deletion 2q14q21

Moshe Frydman, Julia Steinberger, Fiorella Shabtai, Mariassa Bat-Miriam Katznelson, Itzhak Varsano

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 376 KB

english, 1989

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