About us

He established Regentime as a form of spreading the good word to help patients with their incurable diseases and to give hope for their recovery and treatment. Dr. Nassim's work has broadened nationwide with such success and growing. Based in Beirut Lebanon, he travels continuously for further development adding innovations and modifications for the finest results. Abi Chahine is a genuine and approachable physician allowing easy communication methods for questions regarding the use of Regentime treatments for patient satisfaction and peace of mind.

Thus the symbol “∞” indicates the infinite potential of medicine, pointing the new area of regenerative medicine.
An up view of the logo's divisions represent the communication of two people, symbolizing the relationship between doctor and patient, where one of them is giving and the second is receiving aid, in a color combination of green and blue, demonstrating the earth in balance with the endless skies in reflection on the energetic oceans, all in a truthful harmony, indicating optimal health.

Regenerative medicine

Its history goes back to the first human observations about how some female mammals ate their own placenta and umbilical cord after giving birth. These observations lead to a diversity of medical applications in many cultures without knowing exactly the mechanism of action of those biological materials.
As the established MD of this observation, I’m a firm believer that we can gain knowledge and new methods based on what we see in the animal world and applying these methods which are redesigned for the human medical needs that assist in most serious medical conditions.
In today’s healthcare interventions, stem cell therapy has shown to be the next breakthrough in medicine as it has the least or no side effects with effective results.
Stem "blank" cells are capable of becoming specialized cells. They have a remarkable "self-renewal" potential and differentiate into other types of cells; muscular, intestinal, neural, endothelial, blood, retinal, glandular, liver, heart, bone, cartilage, and skin cells.
They can serve as a repair system for the body and its tissues by continuously replenishing other cells in a natural way.
Nassim Halim Abi Chahine

Autologous stem cells are undifferentiated cells found throughout the body. They replenish and renew through cell division and differentiation into specialized cell types. Because of this, stem cells have proven to be effective for organ and tissue restoration and thus, fighting against inoperable diseases.

At this point, most patients would search for just about anything to be treated. Regentime techniques provide healthcare that can relieve symptoms or in some cases resolve the disease itself.
Stem cell transplantation can sometimes exclude the use of some remedies, but most likely the medication is used to support the patients’ condition until further notice.

Further improvement in the patients’ health continues over the following months and years.
Dr. Abi Chahine states; “regeneration is a process, not an event”.

Nevertheless, some methods may lead to slight discomfort related to the massive quantity of stem cells rushing to the treated area. For instance, lumbar infiltration symptoms may range from minimal nausea to some headaches which may last up till one day.
Regentime applicants use the autologous adult bone marrow derived stem cells, which are well known for their safety.

List of Diseases A-Z
2-Hydroxy-glutaric aciduria
2-methylbutyryl CoA deficiency
3-hydroxy-3-methylglutaryl-CoA lyase deficiency
3-Methylcrotonyl-CoA carboxylase deficiency
3-Methylglutaconic aciduria 1
4-Hydroxy-butyric aciduria SSADHD
5-alpha-reductase deficiency
6-Pyruvoyltetrahydropterin synthase deficiency
Acatalasia (Takahara disease)
Activator Deficiency
Acyl-CoA oxidase deficiency
Addison disease
Adrenoleukodystrophy
Adult Refsum disease
Alexander disease
Alkaptonurira
Allan-Herndon-Dudley syndrome
Alpha-mannosidosis
Alpha-methylcayl-CoA racemase deficiency
Aminoacylase 1 deficiency
Amyloidosis
Andersen disease
Anoxic brain damage
Apparent Mineralocorticoid Excess Syndrome
Argininemia
Argininosuccinic aciduria
Aromatase deficiency
Aromatase excess syndrome
Arteriosclerosis
Aspartylglucosaminuria
Asperger syndrome
Asthma
Ataxia
Atherosclerosis
Atopic dermatitis eczema
Atrophic gastritis
Atrophic vaginitis
Autism
Balint syndrome
Batten-Spielmeyer-Sjogren-Vogt
Behcet disease
Bernard-Soulier syndrome
Bests disease
Beta-mannosidosis
Betaketothiolase deficiency
Biotinidase deficiency
Brunner syndrome
Bullous emphysema
Bullous pemphigoid
Burns: classic / thermal / frostbite
Canavan disease
Carbamoyl-phosphate synthase I deficiency
Cardiac insufficiency
Cardiomyopathy
Carnitine palmitoyltransferase deficiency
Carnitine-acylcarnitine translocase deficiency
Carnosenemia
Cerebral amyloid angiopathy
Cerebral palsy
Cerebrotendineous xanthomatosis
Cerebrovascular diseases
Charles Bonnet Syndrome
Chemotherapy side effects and post chemotherapy complications
Childhood disintegrative disorder
Cholesteryl ester storage disease
Chondroplasia: maintenance therapy
Chronic Critical Limb Ischemia
Chronic Hexosaminidase A Deficiency
Citrullinemia
Coenzyme A dehydrogenase deficiency
Color blindness
Cone Rod dystrophy
Congenital adrenal hyperplasia
Congenital dyserythropoietic anemia
Congenital erythropoietic porphyria
Congenital hemolytic anemia nonspherocytic
Congestive heart failure
Cori disease
Coronary artery diseases
Cortical visual impairment
Crigler-Najjar symdrome
Crohn disease
Cystathioninuria
Cystic fibrosis
Cystinosis
D-bifunctional protein deficiency
Danon disease
Dehydroxyacetonephosphate acyltransferase deficiency
Dementia
Dermatomyositis
Diabetes Mellitus type 1
Diabetes Mellitus type 2
Diabetic Neuropathy
Dienoyl-CoA reductase deficiency
Dopamine Beta hydroxylase deficiency
Dubin-Johnson syndrome
Enthesitis chronic
Epilepsy: some types
Ethylmalonic encephalopathy
Fabry disease
Factor V deficiency
Factor X deficiency/Amyloid purpura
Familial alpha-lipoprotein deficiency
Fanconi syndrome/ Oculocerebrorenal syndrome
Fanconi-Bickel syndrome / Glycogen storage disease type XI
Farber disease
Follicle-stimulating hormone insensitivity
Forbes disease
Fructose intolerance
Fucosidosis
Fumarase deficiency
G6PD/ Favism
Galactosemia
Galactosialidosis
Gangliosidosis GM1
Gaucher Disease
Glanzmanns thrombasthenia
Glucocorticoid remedial aldosteronism
Glutaric acidemia
Glycogen storage disease
Gonadotropin-releasing hormone insensitivity
Goodpasture syndrome
Gout severe and recurrent cases
Hartnup disease
Hashimoto thyroiditis refractory cases
Hawkinsinuria
Heart failure
Hemophilia
Hereditary CNS demyelinating disease
Hereditary coproporphyria
Hereditary Fructose intolerance
Hermansky Pudlak syndrome
Hers disease
Hexosaminidase A Deficiency
Histidenemia
Homocystinuria
Hunter syndrome
Huntington disease
Hurler Syndrome
Hyaluronidase Deficiency
Hyperargininemia
Hyperargininuria
Hyperhomocysteinuria
Hyperlysinemias
Hypermethioninemia
Hyperoxaluria/ Bird's disease
Hyperprolinemia
Hypertrophic emphysema
Hypertryptophanemia
Hyperurecemia
Hypervalenemia
Hypo-alpha-lipoproteinemia
Iminoglycinuria
Inborn errors of steroid metabolism
Infantile Free Sialic Acid Storage Disease
Infantile Refsum disease
Interstitial lung disease
Intractable wound healing
Ionizing radiation injury
Isobutyryl-CoA dehydrogenase deficiency
Isolated 17,20-lyase deficiency
Isovaleric acIdemia
Jansky-Bielschowsky disease
Joint regeneration
Juvenile arthritis
Juvenile Hexosaminidase A Deficiency
Kernicterus- Bilirubin encephalopathy
Krabbe disease
Kufs disease
Lactose intolerance
Lebers congenital amaurosis
Lesch-Nyhan syndrome
Leukoencephalopathy
Leukopdystrophies
Leydig cell hypoplasia
Lipoid congenital adrenal hyperplasia
Liver cirrhosis
Locked-in syndrome
Lysinuric protein intolerance
Lysosomal acid lipase deficiency
Lysosomal storage disease
Macular Degeneration
Malonyl-CoA decarboxylase deficiency
Mannosidosis
Maple syrup urine disease
Maroteaux-Lamy syndrome
Menkes disease
Metachromatic Leukodystrophy
Methylmalonic acidemia
Methylmalonyl-CoA mutase deficiency
Mevalonate kinase deficiency/aciduria
Mitochondrial trifunctional protein deficiency
Morquio syndrome
Mucolipidosis all types
Mucopolysaccharidoses disorders
Mulibrey nanism
Multiple Sclerosis
Multiple sulfatase deficiency
Multiple system atrophy
Muscular dystrophy
Myelopathy
Myotonia congenita
N-Acetylglutamate synthase deficiency
Narcolepsy/cataplexy
Neonatal adrenoleukodystrophy
Nephropathy/Glomeronephritis
Neurological Visual Impairment
Neuromyelitis optica
Neuronal Ceroid Lipofuscinoses
Niemann-Pick Disease
Nonketotic hyperglycinemia
Northern Epilepsy syndrome
Obstructive lung disease
Ocular albinism
Optic Nerve Hypoplasia
Ornithine carbamoyltransferase deficiency
Osteomyelitis
Parkinson's disease
Pelizaeus'Merzbacher disease
Pemphigus
Peripheral arterial diseases
Periventricular leukomalacia
Peroxisomal disorder
Peroxisome biogenesis disorders
Pervasive developmental disorder
Phenylketonuria
Pipecolic acedemia/ Hyperpipecolatemia
Polymyositis
Pompe's disease
Porphobilinogen synthase Deficiency
Porphyria cutanea tarda
Primary biliary cirrhosis
Primary carnitine deficiency
Progressive supranuclear palsy
Prolidase deficiency
Propionic acidemia
Pseudo-Hurler polydystrophy
Psoriasis
Psoriatic arthritis
Pulmonary diseases
Pycnodysostosis
Radiation induced lung injury
Radiation injuries Post radiation injuries
Reactive arthritis Reiter's sd
Red cell aldolase deficiency
Refsum disease
Reiters syndrome
Restrictive lung disease
Retinitis Pigmentosa
Retinopathy
Rett syndrome
Rheumatism
Rheumatoid arthritis
Rhizomelic chondrodysplasia punctata
Rotor syndrome
Saccharopinuria
Salla disease
Sandhoff disease
Sanfilippo syndrome
Santavuori-Haltia syndrome
Scheie Syndrome
Schindler disease
Scleroderma
Sialidosis
Sideroblastic anemia
Sj'gren syndrome
Sly Syndrome
Spastic diplegia
Spinal Muscular Atrophy
Stargardts Disease
Stroke
Sturge-Weber Syndrome
Systemic lupus erythematosus
Tangier disease
Tarui's disease
Tay-Sachs disease
Tetrahydrobiopterin deficiency
Thermal radiation injury
Trimethylaminuria/ fish odor syndrome
Tyrosinemia
Ulcerative Colititis
Urocanic aciduria
Usher Syndrome
Variegate porphyria
Vitelliform macular dystrophy
Vitiligo
Von Gierke's disease
Von Willebrand disease
Waardenburg syndrome
Werdnig-Hoffman disease SMA
Wilson's disease
Wolman disease
X-linked adrenoleukodystrophy
Zellweger syndrome
Cases
Activities
FAQ

After hundreds of treated cases, Dr Abi Chahine found that increasing the number of stem cells in their mother location without their mobilization to the circulation is the best way to safely proliferate them, he stated: “the superlative incubator is our bone marrow itself”.
“There is no need to wait more, after almost 48 hours of a Growth factor injection, the human bone marrow becomes saturated with progenitor cells. A peripheral collection of cells from the circulation is always possible after 4-6 days of growth factor injections but it takes longer time and necessitates a complicated procedure.
In the other hand we can always extract stem cells from the source itself, which is the bone marrow, and this is done easily under local anesthesia with or without sedation upon patient’s requirements.

Regentime Procedure starts with the subcutaneous injection of an FDA-approved growth factor. After hundreds of treated cases, Dr Abi Chahine found that increasing the number of stem cells in their mother location without their mobilization to the circulation is the best way to safely proliferate them, he stated: “the superlative incubator is our bone marrow itself”.
“There is no need to wait more, after almost 48 hours of a Growth factor injection, previously used for Leucocytes mobilization, the human bone marrow becomes saturated with progenitor cells.
A peripheral collection of cells from the circulation is always possible after 4-6 days of growth factor injections but it takes longer time and necessitates a complicated procedure. In the other hand we can always extract stem cells from the source itself, which is the bone marrow, and this is done easily under local anesthesia with or without sedation upon patient’s requirements.

2nd day preparation: second growth factor injection.
3rd day: bone marrow collection.
4th day: transplantation of bone marrow and rest after procedure.
5th day: follow up care, resting

Regentime Procedure is individually customized upon each patient’s medical case.

pushed by - defenitively - the longest pioneering experience ever (since 2008), along with the delivery of an excellent service, at the same time, competitive price due to the cheaper costs in our HQ country, will make you choose us

Apply for treatment

Because Bone Marrow Autografts still lacking a code-framing, your doctor tells you what a treatment currently may cost. Cost is the sum of prices of used medications and Lab work. Prices vary depending on severity of disease and usage of products during the transplantation.
In the next few years, prices will be defined but they may be much higher as they will include the medical staff fees.

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Lebanon
00961 3 082 498
info@regentime.com