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Epilepsy surgery series: a study of 502 consecutive patients from a developing country.

Epilepsy research and treatment

Alsemari A, Al-Otaibi F, Baz S, Althubaiti I, Aldhalaan H, Macdonald D, Abalkhail T, Fiol ME, Alyamani S, Chedrawi A, Leblanc F, Parrent A, Maclean D, Girvin J.
PMID: 24627805
Epilepsy Res Treat. 2014;2014:286801. doi: 10.1155/2014/286801. Epub 2014 Jan 30.

Purpose. To review the postoperative seizure outcomes of patients that underwent surgery for epilepsy at King Faisal Specialist Hospital & Research Centre (KFSHRC). Methods. A descriptive retrospective study for 502 patients operated on for medically intractable epilepsy between 1998...

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Alsemari A, Al-Otaibi F, Baz S, et al. Epilepsy surgery series: a study of 502 consecutive patients from a developing country. Epilepsy Res Treat. 2014;2014:286801doi: 10.1155/2014/286801.
Alsemari, A., Al-Otaibi, F., Baz, S., Althubaiti, I., Aldhalaan, H., Macdonald, D., Abalkhail, T., Fiol, M. E., Alyamani, S., Chedrawi, A., Leblanc, F., Parrent, A., Maclean, D., & Girvin, J. (2014). Epilepsy surgery series: a study of 502 consecutive patients from a developing country. Epilepsy research and treatment, 2014286801. https://doi.org/10.1155/2014/286801
Alsemari, Abdulaziz, et al. "Epilepsy surgery series: a study of 502 consecutive patients from a developing country." Epilepsy research and treatment vol. 2014 (2014): 286801. doi: https://doi.org/10.1155/2014/286801
Alsemari A, Al-Otaibi F, Baz S, Althubaiti I, Aldhalaan H, Macdonald D, Abalkhail T, Fiol ME, Alyamani S, Chedrawi A, Leblanc F, Parrent A, Maclean D, Girvin J. Epilepsy surgery series: a study of 502 consecutive patients from a developing country. Epilepsy Res Treat. 2014;2014:286801. doi: 10.1155/2014/286801. Epub 2014 Jan 30. PMID: 24627805; PMCID: PMC3929285.
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Saudi guidelines on the diagnosis and treatment of pulmonary hypertension: 2014 updates.

Annals of thoracic medicine

Idrees MM, Saleemi S, Azem MA, Aldammas S, Alhazmi M, Khan J, Gari A, Aldabbagh M, Sakkijha H, Aldalaan A, Alnajashi K, Alhabeeb W, Nizami I, Kouatli A, Chehab M, Tamimi O, Banjar H, Kashour T, Lopes A, Minai O, Hassoun P, Pasha Q, Mayer E, Butrous G, Bhagavathula S, Ghio S, Swiston J, Boueiz A, Tonelli A, Levy RD, Hoeper M, Levy RD.
PMID: 25076987
Ann Thorac Med. 2014 Jul;9:S1-S15. doi: 10.4103/1817-1737.134006.

The Saudi Association for Pulmonary Hypertension (previously called Saudi Advisory Group for Pulmonary Hypertension) has published the first Saudi Guidelines on Diagnosis and Treatment of Pulmonary Arterial Hypertension back in 2008.[1] That guideline was very detailed and extensive and...

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Idrees MM, Saleemi S, Azem MA, et al. Saudi guidelines on the diagnosis and treatment of pulmonary hypertension: 2014 updates. Ann Thorac Med. 2014;9:S1-S15doi: 10.4103/1817-1737.134006.
Idrees, M. M., Saleemi, S., Azem, M. A., Aldammas, S., Alhazmi, M., Khan, J., Gari, A., Aldabbagh, M., Sakkijha, H., Aldalaan, A., Alnajashi, K., Alhabeeb, W., Nizami, I., Kouatli, A., Chehab, M., Tamimi, O., Banjar, H., Kashour, T., Lopes, A., Minai, O., Hassoun, P., Pasha, Q., Mayer, E., Butrous, G., Bhagavathula, S., Ghio, S., Swiston, J., Boueiz, A., Tonelli, A., Levy, R. D., Hoeper, M., & Levy, R. D. (2014). Saudi guidelines on the diagnosis and treatment of pulmonary hypertension: 2014 updates. Annals of thoracic medicine, 9S1-S15. https://doi.org/10.4103/1817-1737.134006
Idrees, Majdy M, et al. "Saudi guidelines on the diagnosis and treatment of pulmonary hypertension: 2014 updates." Annals of thoracic medicine vol. 9 (2014): S1-S15. doi: https://doi.org/10.4103/1817-1737.134006
Idrees MM, Saleemi S, Azem MA, Aldammas S, Alhazmi M, Khan J, Gari A, Aldabbagh M, Sakkijha H, Aldalaan A, Alnajashi K, Alhabeeb W, Nizami I, Kouatli A, Chehab M, Tamimi O, Banjar H, Kashour T, Lopes A, Minai O, Hassoun P, Pasha Q, Mayer E, Butrous G, Bhagavathula S, Ghio S, Swiston J, Boueiz A, Tonelli A, Levy RD, Hoeper M, Levy RD. Saudi guidelines on the diagnosis and treatment of pulmonary hypertension: 2014 updates. Ann Thorac Med. 2014 Jul;9:S1-S15. doi: 10.4103/1817-1737.134006. PMID: 25076987; PMCID: PMC4114283.
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Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update.

Frontiers in genetics

Maddirevula S, Shamseldin HE, Sirr A, AlAbdi L, Lo RS, Ewida N, Al-Qahtani M, Hashem M, Abdulwahab F, Aboyousef O, Kaya N, Monies D, Salem MH, Al Harbi N, Aldhalaan HM, Alzaidan H, Almanea HM, Alsalamah AK, Al Mutairi F, Ismail S, Abdel-Salam GMH, Alhashem A, Asery A, Faqeih E, AlQassmi A, Al-Hamoudi W, Algoufi T, Shagrani M, Dudley AM, Alkuraya FS.
PMID: 33456446
Front Genet. 2020 Dec 31;11:580484. doi: 10.3389/fgene.2020.580484. eCollection 2020.

There is a growing interest in standardizing gene-disease associations for the purpose of facilitating the proper classification of variants in the context of Mendelian diseases. One key line of evidence is the independent observation of pathogenic variants in unrelated...

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Maddirevula S, Shamseldin HE, Sirr A, et al. Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update. Front Genet. 2020;11:580484doi: 10.3389/fgene.2020.580484.
Maddirevula, S., Shamseldin, H. E., Sirr, A., AlAbdi, L., Lo, R. S., Ewida, N., Al-Qahtani, M., Hashem, M., Abdulwahab, F., Aboyousef, O., Kaya, N., Monies, D., Salem, M. H., Al Harbi, N., Aldhalaan, H. M., Alzaidan, H., Almanea, H. M., Alsalamah, A. K., Al Mutairi, F., Ismail, S., Abdel-Salam, G. M. H., Alhashem, A., Asery, A., Faqeih, E., AlQassmi, A., Al-Hamoudi, W., Algoufi, T., Shagrani, M., Dudley, A. M., & Alkuraya, F. S. (2020). Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update. Frontiers in genetics, 11580484. https://doi.org/10.3389/fgene.2020.580484
Maddirevula, Sateesh, et al. "Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update." Frontiers in genetics vol. 11 (2020): 580484. doi: https://doi.org/10.3389/fgene.2020.580484
Maddirevula S, Shamseldin HE, Sirr A, AlAbdi L, Lo RS, Ewida N, Al-Qahtani M, Hashem M, Abdulwahab F, Aboyousef O, Kaya N, Monies D, Salem MH, Al Harbi N, Aldhalaan HM, Alzaidan H, Almanea HM, Alsalamah AK, Al Mutairi F, Ismail S, Abdel-Salam GMH, Alhashem A, Asery A, Faqeih E, AlQassmi A, Al-Hamoudi W, Algoufi T, Shagrani M, Dudley AM, Alkuraya FS. Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update. Front Genet. 2020 Dec 31;11:580484. doi: 10.3389/fgene.2020.580484. eCollection 2020. PMID: 33456446; PMCID: PMC7806527.
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A Rare Case of Adenosine Deaminase tRNA-Specific 3 Mutation, Adrenal Insufficiency, and Rhabdomyolysis.

Cureus

AlDhalaan W, Syed F, Javaid HA, AlSagheir A, Almustanyir S.
PMID: 34963848
Cureus. 2021 Nov 23;13(11):e19833. doi: 10.7759/cureus.19833. eCollection 2021 Nov.

Adenosine deaminase t-RNA-specific 3 (ADAT3) gene, present on chromosome 19, encodes for an enzyme responsible for deamination of adenosine to inosine. Individuals with ADAT3 mutation display microcephaly, dysmorphic features, neurological, behavioural, and endocrinal pathologies. ADAT3 mutation is a recognized...

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AlDhalaan W, Syed F, Javaid HA, et al. A Rare Case of Adenosine Deaminase tRNA-Specific 3 Mutation, Adrenal Insufficiency, and Rhabdomyolysis. Cureus. 2021;13(11):e19833doi: 10.7759/cureus.19833.
AlDhalaan, W., Syed, F., Javaid, H. A., AlSagheir, A., & Almustanyir, S. (2021). A Rare Case of Adenosine Deaminase tRNA-Specific 3 Mutation, Adrenal Insufficiency, and Rhabdomyolysis. Cureus, 13(11), e19833. https://doi.org/10.7759/cureus.19833
AlDhalaan, Waheeb, et al. "A Rare Case of Adenosine Deaminase tRNA-Specific 3 Mutation, Adrenal Insufficiency, and Rhabdomyolysis." Cureus vol. 13,11 (2021): e19833. doi: https://doi.org/10.7759/cureus.19833
AlDhalaan W, Syed F, Javaid HA, AlSagheir A, Almustanyir S. A Rare Case of Adenosine Deaminase tRNA-Specific 3 Mutation, Adrenal Insufficiency, and Rhabdomyolysis. Cureus. 2021 Nov 23;13(11):e19833. doi: 10.7759/cureus.19833. eCollection 2021 Nov. PMID: 34963848; PMCID: PMC8702390.
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Saudi guidelines on the diagnosis and treatment of pulmonary hypertension: 2014 updates.

Annals of thoracic medicine

Idrees MM, Saleemi S, Azem MA, Aldammas S, Alhazmi M, Khan J, Gari A, Aldabbagh M, Sakkijha H, Aldalaan A, Alnajashi K, Alhabeeb W, Nizami I, Kouatli A, Chehab M, Tamimi O, Banjar H, Kashour T, Lopes A, Minai O, Hassoun P, Pasha Q, Mayer E, Butrous G, Bhagavathula S, Ghio S, Swiston J, Boueiz A, Tonelli A, Levy RD, Hoeper M, Levy RD.
PMID: 25076987
Ann Thorac Med. 2014 Jul;9:S1-S15. doi: 10.4103/1817-1737.134006.

The Saudi Association for Pulmonary Hypertension (previously called Saudi Advisory Group for Pulmonary Hypertension) has published the first Saudi Guidelines on Diagnosis and Treatment of Pulmonary Arterial Hypertension back in 2008.[1] That guideline was very detailed and extensive and...

Cite
Idrees MM, Saleemi S, Azem MA, et al. Saudi guidelines on the diagnosis and treatment of pulmonary hypertension: 2014 updates. Ann Thorac Med. 2014;9:S1-S15doi: 10.4103/1817-1737.134006.
Idrees, M. M., Saleemi, S., Azem, M. A., Aldammas, S., Alhazmi, M., Khan, J., Gari, A., Aldabbagh, M., Sakkijha, H., Aldalaan, A., Alnajashi, K., Alhabeeb, W., Nizami, I., Kouatli, A., Chehab, M., Tamimi, O., Banjar, H., Kashour, T., Lopes, A., Minai, O., Hassoun, P., Pasha, Q., Mayer, E., Butrous, G., Bhagavathula, S., Ghio, S., Swiston, J., Boueiz, A., Tonelli, A., Levy, R. D., Hoeper, M., & Levy, R. D. (2014). Saudi guidelines on the diagnosis and treatment of pulmonary hypertension: 2014 updates. Annals of thoracic medicine, 9S1-S15. https://doi.org/10.4103/1817-1737.134006
Idrees, Majdy M, et al. "Saudi guidelines on the diagnosis and treatment of pulmonary hypertension: 2014 updates." Annals of thoracic medicine vol. 9 (2014): S1-S15. doi: https://doi.org/10.4103/1817-1737.134006
Idrees MM, Saleemi S, Azem MA, Aldammas S, Alhazmi M, Khan J, Gari A, Aldabbagh M, Sakkijha H, Aldalaan A, Alnajashi K, Alhabeeb W, Nizami I, Kouatli A, Chehab M, Tamimi O, Banjar H, Kashour T, Lopes A, Minai O, Hassoun P, Pasha Q, Mayer E, Butrous G, Bhagavathula S, Ghio S, Swiston J, Boueiz A, Tonelli A, Levy RD, Hoeper M, Levy RD. Saudi guidelines on the diagnosis and treatment of pulmonary hypertension: 2014 updates. Ann Thorac Med. 2014 Jul;9:S1-S15. doi: 10.4103/1817-1737.134006. PMID: 25076987; PMCID: PMC4114283.
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Tuberous Sclerosis Complex: Clinical Spectrum and Epilepsy: A Retrospective Chart Review Study.

Translational neuroscience

Almobarak S, Almuhaizea M, Abukhaled M, Alyamani S, Dabbagh O, Chedrawi A, Khan S, Aldhalaan H.
PMID: 30479846
Transl Neurosci. 2018 Nov 12;9:154-160. doi: 10.1515/tnsci-2018-0023. eCollection 2018.

Tuberous sclerosis complex (TSC) is an autosomal dominant genetic neurocutaneous disorder, with heterogeneous manifestations. We aimed to review the clinical presentation of TSC and its association with epilepsy among Saudi population. This was a retrospective chart review study of...

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Almobarak S, Almuhaizea M, Abukhaled M, et al. Tuberous Sclerosis Complex: Clinical Spectrum and Epilepsy: A Retrospective Chart Review Study. Transl Neurosci. 2018;9:154-160doi: 10.1515/tnsci-2018-0023.
Almobarak, S., Almuhaizea, M., Abukhaled, M., Alyamani, S., Dabbagh, O., Chedrawi, A., Khan, S., & Aldhalaan, H. (2018). Tuberous Sclerosis Complex: Clinical Spectrum and Epilepsy: A Retrospective Chart Review Study. Translational neuroscience, 9154-160. https://doi.org/10.1515/tnsci-2018-0023
Almobarak, Sulaiman, et al. "Tuberous Sclerosis Complex: Clinical Spectrum and Epilepsy: A Retrospective Chart Review Study." Translational neuroscience vol. 9 (2018): 154-160. doi: https://doi.org/10.1515/tnsci-2018-0023
Almobarak S, Almuhaizea M, Abukhaled M, Alyamani S, Dabbagh O, Chedrawi A, Khan S, Aldhalaan H. Tuberous Sclerosis Complex: Clinical Spectrum and Epilepsy: A Retrospective Chart Review Study. Transl Neurosci. 2018 Nov 12;9:154-160. doi: 10.1515/tnsci-2018-0023. eCollection 2018. PMID: 30479846; PMCID: PMC6234476.
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Effects of early and recent mercury and lead exposure on the neurodevelopment of children with elevated mercury and/or developmental delays during lactation: A follow-up study.

International journal of hygiene and environmental health

Al-Saleh I, Moncari L, Jomaa A, Elkhatib R, Al-Rouqi R, Eltabache C, Al-Rajudi T, Alnuwaysir H, Nester M, Aldhalaan H.
PMID: 32956901
Int J Hyg Environ Health. 2020 Sep;230:113629. doi: 10.1016/j.ijheh.2020.113629. Epub 2020 Sep 18.

This follow-up study of 82 children investigated the potential impact of early and recent exposure to mercury and lead on their neurodevelopmental performance at 5-8 years of age (2017-2018). Early exposure of these children to mercury, methylmercury, and lead...

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Al-Saleh I, Moncari L, Jomaa A, et al. Effects of early and recent mercury and lead exposure on the neurodevelopment of children with elevated mercury and/or developmental delays during lactation: A follow-up study. Int J Hyg Environ Health. 2020;230:113629doi: 10.1016/j.ijheh.2020.113629.
Al-Saleh, I., Moncari, L., Jomaa, A., Elkhatib, R., Al-Rouqi, R., Eltabache, C., Al-Rajudi, T., Alnuwaysir, H., Nester, M., & Aldhalaan, H. (2020). Effects of early and recent mercury and lead exposure on the neurodevelopment of children with elevated mercury and/or developmental delays during lactation: A follow-up study. International journal of hygiene and environmental health, 230113629. https://doi.org/10.1016/j.ijheh.2020.113629
Al-Saleh, Iman, et al. "Effects of early and recent mercury and lead exposure on the neurodevelopment of children with elevated mercury and/or developmental delays during lactation: A follow-up study." International journal of hygiene and environmental health vol. 230 (2020): 113629. doi: https://doi.org/10.1016/j.ijheh.2020.113629
Al-Saleh I, Moncari L, Jomaa A, Elkhatib R, Al-Rouqi R, Eltabache C, Al-Rajudi T, Alnuwaysir H, Nester M, Aldhalaan H. Effects of early and recent mercury and lead exposure on the neurodevelopment of children with elevated mercury and/or developmental delays during lactation: A follow-up study. Int J Hyg Environ Health. 2020 Sep;230:113629. doi: 10.1016/j.ijheh.2020.113629. Epub 2020 Sep 18. PMID: 32956901.
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Isolated Congenital Supernumerary Nostril in an Adult Patient.

Ear, nose, & throat journal

Alqabbani AA, Alateeq MF, Alshalaan Z.
PMID: 32551959
Ear Nose Throat J. 2021 Dec;100(10):1038S-1040S. doi: 10.1177/0145561320933390. Epub 2020 Jun 18.

The supernumerary nostril is a congenital accessory nostril, which is considered to be one of the rarest congenital nasal anomalies with an unknown etiology. We present the first case of a supernumerary nostril in an adult Saudi patient, which...

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Alqabbani AA, Alateeq MF, Alshalaan Z. Isolated Congenital Supernumerary Nostril in an Adult Patient. Ear Nose Throat J. 2020;100(10):1038S-1040Sdoi: 10.1177/0145561320933390.
Alqabbani, A. A., Alateeq, M. F., & Alshalaan, Z. (2021). Isolated Congenital Supernumerary Nostril in an Adult Patient. Ear, nose, & throat journal, 100(10), 1038S-1040S. https://doi.org/10.1177/0145561320933390
Alqabbani, Almaha A, et al. "Isolated Congenital Supernumerary Nostril in an Adult Patient." Ear, nose, & throat journal vol. 100,10 (2021): 1038S-1040S. doi: https://doi.org/10.1177/0145561320933390
Alqabbani AA, Alateeq MF, Alshalaan Z. Isolated Congenital Supernumerary Nostril in an Adult Patient. Ear Nose Throat J. 2021 Dec;100(10):1038S-1040S. doi: 10.1177/0145561320933390. Epub 2020 Jun 18. PMID: 32551959.
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Medication-related Osteonecrosis of the Jaw: A Review.

Cureus

AlDhalaan NA, BaQais A, Al-Omar A.
PMID: 32190495
Cureus. 2020 Feb 10;12(2):e6944. doi: 10.7759/cureus.6944.

Medication-related osteonecrosis of the jaw (MRONJ) is a rare, severe debilitating condition from unknown causes. It is characterized by nonhealing exposed bone in a patient with a history of antiresorptive or antiangiogenic agents in the absence of radiation exposure...

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AlDhalaan NA, BaQais A, Al-Omar A. Medication-related Osteonecrosis of the Jaw: A Review. Cureus. 2020;12(2):e6944doi: 10.7759/cureus.6944.
AlDhalaan, N. A., BaQais, A., & Al-Omar, A. (2020). Medication-related Osteonecrosis of the Jaw: A Review. Cureus, 12(2), e6944. https://doi.org/10.7759/cureus.6944
AlDhalaan, Nouf A, et al. "Medication-related Osteonecrosis of the Jaw: A Review." Cureus vol. 12,2 (2020): e6944. doi: https://doi.org/10.7759/cureus.6944
AlDhalaan NA, BaQais A, Al-Omar A. Medication-related Osteonecrosis of the Jaw: A Review. Cureus. 2020 Feb 10;12(2):e6944. doi: 10.7759/cureus.6944. PMID: 32190495; PMCID: PMC7067354.
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Stigmatization among parents of autism spectrum disorder children in Riyadh, Saudi Arabia.

International journal of pediatrics & adolescent medicine

Alshaigi K, Albraheem R, Alsaleem K, Zakaria M, Jobeir A, Aldhalaan H.
PMID: 33094144
Int J Pediatr Adolesc Med. 2020 Sep;7(3):140-146. doi: 10.1016/j.ijpam.2019.06.003. Epub 2019 Jun 17.

BACKGROUND: Children diagnosed with autism spectrum disorder (ASD) have social and cognitive disabilities. For parents, these behaviors can lead to humiliation, social exclusion, and isolation. Stigma is a problem that not only may affect the individual with high functioning...

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Alshaigi K, Albraheem R, Alsaleem K, et al. Stigmatization among parents of autism spectrum disorder children in Riyadh, Saudi Arabia. Int J Pediatr Adolesc Med. 2019;7(3):140-146doi: 10.1016/j.ijpam.2019.06.003.
Alshaigi, K., Albraheem, R., Alsaleem, K., Zakaria, M., Jobeir, A., & Aldhalaan, H. (2020). Stigmatization among parents of autism spectrum disorder children in Riyadh, Saudi Arabia. International journal of pediatrics & adolescent medicine, 7(3), 140-146. https://doi.org/10.1016/j.ijpam.2019.06.003
Alshaigi, Kahlid, et al. "Stigmatization among parents of autism spectrum disorder children in Riyadh, Saudi Arabia." International journal of pediatrics & adolescent medicine vol. 7,3 (2020): 140-146. doi: https://doi.org/10.1016/j.ijpam.2019.06.003
Alshaigi K, Albraheem R, Alsaleem K, Zakaria M, Jobeir A, Aldhalaan H. Stigmatization among parents of autism spectrum disorder children in Riyadh, Saudi Arabia. Int J Pediatr Adolesc Med. 2020 Sep;7(3):140-146. doi: 10.1016/j.ijpam.2019.06.003. Epub 2019 Jun 17. PMID: 33094144; PMCID: PMC7568054.
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Adapting evidence-based clinical practice guidelines for people with attention deficit hyperactivity disorder in Saudi Arabia: process and outputs of a national initiative.

Child and adolescent psychiatry and mental health

Bashiri FA, Albatti TH, Hamad MH, Al-Joudi HF, Daghash HF, Al-Salehi SM, Varnham JL, Alhaidar F, Almodayfer O, Alhossein A, Aldhalaan H, Ad-Dab'bagh YA, Al Backer N, Altwaijri W, Alburikan K, Buraik MW, Ghaziuddin M, Nester MJ, Wahabi HA, Alhabib S, Jamal AA, Amer YS.
PMID: 33557914
Child Adolesc Psychiatry Ment Health. 2021 Feb 08;15(1):6. doi: 10.1186/s13034-020-00351-5.

BACKGROUND: We recently adapted the published National Institute for Health and Care Excellence (NICE) Attention deficit hyperactivity disorder (ADHD) diagnosis and management guideline to the Saudi Arabian context. It has been postulated that adaptation of evidence-based clinical practice guidelines...

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Bashiri FA, Albatti TH, Hamad MH, et al. Adapting evidence-based clinical practice guidelines for people with attention deficit hyperactivity disorder in Saudi Arabia: process and outputs of a national initiative. Child Adolesc Psychiatry Ment Health. 2021;15(1):6doi: 10.1186/s13034-020-00351-5.
Bashiri, F. A., Albatti, T. H., Hamad, M. H., Al-Joudi, H. F., Daghash, H. F., Al-Salehi, S. M., Varnham, J. L., Alhaidar, F., Almodayfer, O., Alhossein, A., Aldhalaan, H., Ad-Dab'bagh, Y. A., Al Backer, N., Altwaijri, W., Alburikan, K., Buraik, M. W., Ghaziuddin, M., Nester, M. J., Wahabi, H. A., Alhabib, S., Jamal, A. A., & Amer, Y. S. (2021). Adapting evidence-based clinical practice guidelines for people with attention deficit hyperactivity disorder in Saudi Arabia: process and outputs of a national initiative. Child and adolescent psychiatry and mental health, 15(1), 6. https://doi.org/10.1186/s13034-020-00351-5
Bashiri, Fahad A, et al. "Adapting evidence-based clinical practice guidelines for people with attention deficit hyperactivity disorder in Saudi Arabia: process and outputs of a national initiative." Child and adolescent psychiatry and mental health vol. 15,1 (2021): 6. doi: https://doi.org/10.1186/s13034-020-00351-5
Bashiri FA, Albatti TH, Hamad MH, Al-Joudi HF, Daghash HF, Al-Salehi SM, Varnham JL, Alhaidar F, Almodayfer O, Alhossein A, Aldhalaan H, Ad-Dab'bagh YA, Al Backer N, Altwaijri W, Alburikan K, Buraik MW, Ghaziuddin M, Nester MJ, Wahabi HA, Alhabib S, Jamal AA, Amer YS. Adapting evidence-based clinical practice guidelines for people with attention deficit hyperactivity disorder in Saudi Arabia: process and outputs of a national initiative. Child Adolesc Psychiatry Ment Health. 2021 Feb 08;15(1):6. doi: 10.1186/s13034-020-00351-5. PMID: 33557914; PMCID: PMC7871371.
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A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report.

Journal of medical case reports

Abu-Amero KK, Al-Dhalaan H, Bohlega S, Hellani A, Taylor RW.
PMID: 19946553
J Med Case Rep. 2009 Oct 15;3:77. doi: 10.1186/1752-1947-3-77.

INTRODUCTION: There are currently 23 missense point mutations and one 4 basepair deletion spanning different mitochondrial genes associated with mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS). The spectrum of mitochondrial DNA mutations in Arab patients with MELAS is...

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Abu-Amero KK, Al-Dhalaan H, Bohlega S, et al. A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report. J Med Case Rep. 2009;3:77doi: 10.1186/1752-1947-3-77.
Abu-Amero, K. K., Al-Dhalaan, H., Bohlega, S., Hellani, A., & Taylor, R. W. (2009). A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report. Journal of medical case reports, 377. https://doi.org/10.1186/1752-1947-3-77
Abu-Amero, Khaled K, et al. "A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report." Journal of medical case reports vol. 3 (2009): 77. doi: https://doi.org/10.1186/1752-1947-3-77
Abu-Amero KK, Al-Dhalaan H, Bohlega S, Hellani A, Taylor RW. A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report. J Med Case Rep. 2009 Oct 15;3:77. doi: 10.1186/1752-1947-3-77. PMID: 19946553; PMCID: PMC2783076.
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Showing 1 to 12 of 34 entries